A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966862



Internal ID18602091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98384492..98387090hg38UCSC Ensembl
Innerchr7:98013804..98016402hg19UCSC Ensembl
Innerchr7:97851740..97854338hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2470440, nssv2470441, nssv2470439, nssv2470444, nssv2470436, nssv2470442, nssv2470438, nssv2470435, nssv2470443, nssv2470437
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesBAIAP2L1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966862
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