A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977720



Internal ID18612926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58865245..58873174hg38UCSC Ensembl
Innerchr15:59157444..59165373hg19UCSC Ensembl
Innerchr15:56944736..56952665hg18UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg387930
hg197930
hg187930
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2025169, nssv2025173, nssv2025170, nssv2025167, nssv2025168, nssv2025174, nssv2025171, nssv2025172, nssv2025175, nssv2025176
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)nsv977720
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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