A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947858



Internal ID18594705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38227648..38343325hg38UCSC Ensembl
Innerchr10:38516576..38632253hg19UCSC Ensembl
Innerchr10:38556582..38672259hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38115678
hg19115678
hg18115678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1842332, nssv1842337, nssv1842335, nssv1842331, nssv1842330, nssv1842333, nssv1842338, nssv1842339, nssv1842336, nssv1842334
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)nsv947858
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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