A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964104



Internal ID18252656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151100977..151107733hg38UCSC Ensembl
Innerchr4:152022129..152028885hg19UCSC Ensembl
Innerchr4:152241579..152248335hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg386757
hg196757
hg186757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2336735, nssv2336734, nssv2336736, nssv2336737, nssv2336732, nssv2336739, nssv2336741, nssv2336733, nssv2336738, nssv2336740
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPS3A, SNORD73A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964104
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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