A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977702



Internal ID18612908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40760551..40761148hg38UCSC Ensembl
Innerchr15:41052749..41053346hg19UCSC Ensembl
Innerchr15:38840041..38840638hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38598
hg19598
hg18598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2019361, nssv2019367, nssv2019364, nssv2019368, nssv2019369, nssv2019360, nssv2019366, nssv2019365, nssv2019362, nssv2019363
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)nsv977702
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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