A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947977



Internal ID18248137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48743489..48745836hg38UCSC Ensembl
Innerchr10:49951534..49953881hg19UCSC Ensembl
Innerchr10:49621540..49623887hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382348
hg192348
hg182348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1847581, nssv1847585, nssv1847589, nssv1847588, nssv1847586, nssv1847587, nssv1847582, nssv1847580, nssv1847584, nssv1847583
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesWDFY4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947977
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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