A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984035



Internal ID18619225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28211180..28244658hg38UCSC Ensembl
Innerchr15:28456326..28489804hg19UCSC Ensembl
Innerchr15:26129921..26163399hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3833479
hg1933479
hg1833479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2010603, nssv2010606, nssv2010609, nssv2010610, nssv2010607, nssv2010604, nssv2010612, nssv2010605, nssv2010608, nssv2010611
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984035
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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