A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967741



Internal ID18256283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40785965..40789990hg38UCSC Ensembl
Innerchr4:40787982..40792007hg19UCSC Ensembl
Innerchr4:40482739..40486764hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384026
hg194026
hg184026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2317855, nssv2317854, nssv2317858, nssv2317857, nssv2317852, nssv2317856, nssv2317851, nssv2317850, nssv2317853, nssv2317849
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNSUN7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967741
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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