A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947996



Internal ID18248156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45902056..45909652hg38UCSC Ensembl
Innerchr10:51686174..51693770hg19UCSC Ensembl
Innerchr10:51356180..51363776hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg387597
hg197597
hg187597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1847995, nssv1847991, nssv1847993, nssv1847998, nssv1847994, nssv1847990, nssv1847996, nssv1847999, nssv1847997, nssv1847992
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)nsv947996
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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