A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967730



Internal ID18602958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19813741..19816026hg38UCSC Ensembl
Innerchr4:19815364..19817649hg19UCSC Ensembl
Innerchr4:19424462..19426747hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg382286
hg192286
hg182286
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2312839, nssv2312841, nssv2312846, nssv2312844, nssv2312842, nssv2312840, nssv2312837, nssv2312845, nssv2312843, nssv2312838
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)nsv967730
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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