A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976903



Internal ID18612109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28198679..28203916hg38UCSC Ensembl
Innerchr15:28443825..28449062hg19UCSC Ensembl
Innerchr15:26117420..26122657hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg385238
hg195238
hg185238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2010539, nssv2010541, nssv2010540, nssv2010542, nssv2010538, nssv2010534, nssv2010536, nssv2010533, nssv2010537, nssv2010535
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)nsv976903
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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