A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974525



Internal ID18609736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22533639..22565685hg38UCSC Ensembl
Innerchr15:23307411..23339457hg19UCSC Ensembl
Innerchr15:20858852..20890898hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3832047
hg1932047
hg1832047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2007625, nssv2007622, nssv2007620, nssv2007617, nssv2007619, nssv2007623, nssv2007621, nssv2007626, nssv2007624, nssv2007618
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974525
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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