A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964044



Internal ID18599282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:45005635..45032450hg38UCSC Ensembl
Innerchr4:45007652..45034467hg19UCSC Ensembl
Innerchr4:44702409..44729224hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3826816
hg1926816
hg1826816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2318180, nssv2318181, nssv2318182, nssv2318186, nssv2318178, nssv2318187, nssv2318179, nssv2318183, nssv2318184, nssv2318185
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)nsv964044
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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