A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966331



Internal ID18601561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155451748..155466099hg38UCSC Ensembl
Innerchr4:156372900..156387251hg19UCSC Ensembl
Innerchr4:156592350..156606701hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3814352
hg1914352
hg1814352
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2339003, nssv2339002, nssv2338995, nssv2338998, nssv2339001, nssv2338999, nssv2338994, nssv2339000, nssv2338997, nssv2338996
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)nsv966331
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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