A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964082



Internal ID18599320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:110480519..110492066hg38UCSC Ensembl
Innerchr4:111401675..111413222hg19UCSC Ensembl
Innerchr4:111621124..111632671hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3811548
hg1911548
hg1811548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2331440, nssv2331431, nssv2331438, nssv2331435, nssv2331434, nssv2331432, nssv2331433, nssv2331436, nssv2331437, nssv2331439
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesENPEP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964082
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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