A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976905



Internal ID18612111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28291680..28297073hg38UCSC Ensembl
Innerchr15:28536826..28542219hg19UCSC Ensembl
Innerchr15:26210421..26215814hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg385394
hg195394
hg185394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2011422, nssv2011427, nssv2011431, nssv2011428, nssv2011423, nssv2011425, nssv2011429, nssv2011426, nssv2011424, nssv2011430
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)nsv976905
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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