A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976965



Internal ID18612171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93061784..93063421hg38UCSC Ensembl
Innerchr15:93605013..93606650hg19UCSC Ensembl
Innerchr15:91406017..91407654hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381638
hg191638
hg181638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2038184, nssv2038177, nssv2038180, nssv2038183, nssv2038181, nssv2038179, nssv2038185, nssv2038186, nssv2038178, nssv2038182
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRGMA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976965
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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