A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947981



Internal ID18594827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49815157..49817527hg38UCSC Ensembl
Innerchr10:51023203..51025573hg19UCSC Ensembl
Innerchr10:50693209..50695579hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382371
hg192371
hg182371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1848235, nssv1848238, nssv1848234, nssv1848233, nssv1848236, nssv1848237, nssv1848241, nssv1848239, nssv1848232, nssv1848240
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)nsv947981
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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