A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966337



Internal ID18601567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165236795..165255209hg38UCSC Ensembl
Innerchr4:166157947..166176361hg19UCSC Ensembl
Innerchr4:166377397..166395811hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3818415
hg1918415
hg1818415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2339860, nssv2339854, nssv2339862, nssv2339856, nssv2339859, nssv2339855, nssv2339857, nssv2339863, nssv2339861, nssv2339858
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKLHL2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966337
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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