A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947871



Internal ID18594718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42107873..42181234hg38UCSC Ensembl
Innerchr10:42603321..42676682hg19UCSC Ensembl
Innerchr10:41923327..41996688hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3873362
hg1973362
hg1873362
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1840593, nssv1840594, nssv1840591, nssv1840598, nssv1840595, nssv1840597, nssv1840592, nssv1840589, nssv1840596, nssv1840590
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947871
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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