A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984080



Internal ID18619270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59677096..59677698hg38UCSC Ensembl
Innerchr15:59969295..59969897hg19UCSC Ensembl
Innerchr15:57756587..57757189hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38603
hg19603
hg18603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2026482, nssv2026488, nssv2026490, nssv2026485, nssv2026484, nssv2026483, nssv2026489, nssv2026491, nssv2026486, nssv2026487
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesBNIP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984080
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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