A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967751



Internal ID18602979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64607485..64608581hg38UCSC Ensembl
Innerchr4:65473203..65474299hg19UCSC Ensembl
Innerchr4:65155798..65156894hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381097
hg191097
hg181097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2319821, nssv2319824, nssv2319819, nssv2319822, nssv2319818, nssv2319825, nssv2319820, nssv2319817, nssv2319823, nssv2319816
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)nsv967751
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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