A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977679



Internal ID18612885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28144706..28146627hg38UCSC Ensembl
Innerchr15:28389852..28391773hg19UCSC Ensembl
Innerchr15:26063447..26065368hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381922
hg191922
hg181922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2014388, nssv2014387, nssv2014389, nssv2014382, nssv2014384, nssv2014391, nssv2014386, nssv2014385, nssv2014390, nssv2014383
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977679
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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