A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967777



Internal ID18603005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99988598..99992035hg38UCSC Ensembl
Innerchr4:100909755..100913192hg19UCSC Ensembl
Innerchr4:101128778..101132215hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg383438
hg193438
hg183438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2330309, nssv2330312, nssv2330310, nssv2330311, nssv2330305, nssv2330308, nssv2330303, nssv2330306, nssv2330304, nssv2330307
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)nsv967777
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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