A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948264



Internal ID18595110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38472039..38529907hg38UCSC Ensembl
Innerchr10:38760967..38818835hg19UCSC Ensembl
Innerchr10:38800973..38859132hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3857869
hg1957869
hg1858160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv21n82
Supporting Variantsnssv2607234, nssv2607230, nssv2607232, nssv2607229, nssv2607235, nssv2607231, nssv2607236, nssv2607238, nssv2607233, nssv2607237
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948264
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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