A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966322



Internal ID18601552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:136350846..136356101hg38UCSC Ensembl
Innerchr4:137272001..137277256hg19UCSC Ensembl
Innerchr4:137491451..137496706hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg385256
hg195256
hg185256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2336612, nssv2336605, nssv2336608, nssv2336611, nssv2336607, nssv2336610, nssv2336606, nssv2336614, nssv2336609, nssv2336613
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)nsv966322
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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