A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv585683

Internal ID

16373092

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr20:19924061..19924613	hg38	UCSC Ensembl
Inner	chr20:19904705..19905257	hg19	UCSC Ensembl
Inner	chr20:19852705..19853257	hg18	UCSC Ensembl

Cytoband

20p11.23

Allele length

Assembly	Allele length
hg38	553
hg19	553
hg18	553

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv938657, nssv938712, nssv938694, nssv938719, nssv938661, nssv938684, nssv938729, nssv938648, nssv938697, nssv938683, nssv938723, nssv938665, nssv938718, nssv938701, nssv938671, nssv938637, nssv938663, nssv938655, nssv938698, nssv938682, nssv938673, nssv938681, nssv938692, nssv938716, nssv938689, nssv938647, nssv938704, nssv938699, nssv938646, nssv938734, nssv938731, nssv938679, nssv938676, nssv938703, nssv938695, nssv938715, nssv938713, nssv938654, nssv938693, nssv938711, nssv938696, nssv938669, nssv938724, nssv938688, nssv938726, nssv938674, nssv938640, nssv938668, nssv938733, nssv938705, nssv938639, nssv938664, nssv938722, nssv938730, nssv938658, nssv938706, nssv938656, nssv938685, nssv938641, nssv938720, nssv938642, nssv938721, nssv938675, nssv938680, nssv938708, nssv938709, nssv938643, nssv938677, nssv938644, nssv938659, nssv938717, nssv938678, nssv938662, nssv938702, nssv938649, nssv938728, nssv938725, nssv938710, nssv938714, nssv938660, nssv938666, nssv938651, nssv938700, nssv938672, nssv938732, nssv938653, nssv938650, nssv938690, nssv938691, nssv938707, nssv938645, nssv938670, nssv938638, nssv938686, nssv938667, nssv938687, nssv938727, nssv938652

Samples

Known Genes

Method

SNP array

Analysis

Illumina SNP array copy number analysis

Platform

Not reported

Comments

Reference

Cooper_et_al_2011

Pubmed ID

Accession Number(s)

Frequency

Sample Size	17421
Observed Gain	76
Observed Loss	22
Observed Complex	0
Frequency	n/a