A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974538



Internal ID18609749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28312772..28316631hg38UCSC Ensembl
Innerchr15:28557918..28561777hg19UCSC Ensembl
Innerchr15:26231513..26235372hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg383860
hg193860
hg183860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2012581, nssv2012586, nssv2012578, nssv2012584, nssv2012585, nssv2012583, nssv2012582, nssv2012577, nssv2012579, nssv2012580
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974538
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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