A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976921



Internal ID18265441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35237003..35237708hg38UCSC Ensembl
Innerchr15:35529204..35529909hg19UCSC Ensembl
Innerchr15:33316496..33317201hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2016803, nssv2016794, nssv2016798, nssv2016799, nssv2016801, nssv2016797, nssv2016796, nssv2016795, nssv2016802, nssv2016800
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANP32AP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976921
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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