A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967725



Internal ID18602953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13336342..13338407hg38UCSC Ensembl
Innerchr4:13337966..13340031hg19UCSC Ensembl
Innerchr4:12947064..12949129hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382066
hg192066
hg182066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2312221, nssv2312225, nssv2312224, nssv2312228, nssv2312222, nssv2312219, nssv2312227, nssv2312223, nssv2312220, nssv2312226
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)nsv967725
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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