A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980197



Internal ID18615397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:41841327..41843966hg38UCSC Ensembl
Innerchr4:41843344..41845983hg19UCSC Ensembl
Innerchr4:41538101..41540740hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382640
hg192640
hg182640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2317946, nssv2317951, nssv2317950, nssv2317953, nssv2317954, nssv2317955, nssv2317947, nssv2317948, nssv2317952, nssv2317949
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)nsv980197
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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