A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974535



Internal ID18609746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25946718..25954534hg38UCSC Ensembl
Innerchr15:26191865..26199681hg19UCSC Ensembl
Innerchr15:23742958..23750774hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg387817
hg197817
hg187817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2012950, nssv2012953, nssv2012958, nssv2012956, nssv2012955, nssv2012954, nssv2012952, nssv2012959, nssv2012951, nssv2012957
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100128714
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974535
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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