A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977109



Internal ID18612315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11926165..11947988hg38UCSC Ensembl
Innerchr16:12020022..12041845hg19UCSC Ensembl
Innerchr16:11927523..11949346hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3821824
hg1921824
hg1821824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2044733, nssv2044736, nssv2044740, nssv2044735, nssv2044739, nssv2044737, nssv2044742, nssv2044741, nssv2044738, nssv2044734
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977109
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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