A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976922



Internal ID18612128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36613191..36615800hg38UCSC Ensembl
Innerchr15:36905392..36908001hg19UCSC Ensembl
Innerchr15:34692684..34695293hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382610
hg192610
hg182610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2017788, nssv2017785, nssv2017783, nssv2017787, nssv2017780, nssv2017786, nssv2017789, nssv2017782, nssv2017781, nssv2017784
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC15orf41
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976922
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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