A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968873



Internal ID18604101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7281630..7311773hg38UCSC Ensembl
Innerchr5:7281743..7311886hg19UCSC Ensembl
Innerchr5:7334743..7364886hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3830144
hg1930144
hg1830144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2345704, nssv2345702, nssv2345701, nssv2345708, nssv2345707, nssv2345709, nssv2345703, nssv2345710, nssv2345706, nssv2345705
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC442132
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968873
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer