A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947957



Internal ID18248117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50152720..50199367hg38UCSC Ensembl
Innerchr10:47967181..48013835hg19UCSC Ensembl
Innerchr10:47487187..47533841hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3846648
hg1946655
hg1846655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1855350, nssv1855344, nssv1855345, nssv1855343, nssv1855342, nssv1855348, nssv1855349, nssv1855346, nssv1855341, nssv1855347
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947957
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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