A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966265



Internal ID18254809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:47491019..47491632hg38UCSC Ensembl
Innerchr4:47493036..47493649hg19UCSC Ensembl
Innerchr4:47187793..47188406hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38614
hg19614
hg18614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2317756, nssv2317753, nssv2317761, nssv2317759, nssv2317754, nssv2317758, nssv2317755, nssv2317757, nssv2317760, nssv2317752
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesATP10D
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966265
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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