A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971761



Internal ID18260292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49988703..49990996hg38UCSC Ensembl
Innerchr10:51748463..51750756hg19UCSC Ensembl
Innerchr10:51418469..51420762hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382294
hg192294
hg182294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2614367, nssv2614369, nssv2614373, nssv2614368, nssv2614366, nssv2614372, nssv2614374, nssv2614371, nssv2614370, nssv2614365
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesAGAP6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971761
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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