A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947857



Internal ID18594704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38165023..38208712hg38UCSC Ensembl
Innerchr10:38453951..38497640hg19UCSC Ensembl
Innerchr10:38493957..38537646hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3843690
hg1943690
hg1843690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1841318, nssv1841310, nssv1841317, nssv1841309, nssv1841315, nssv1841314, nssv1841312, nssv1841311, nssv1841316, nssv1841313
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100129055
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947857
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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