A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966302



Internal ID18601532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102461277..102463703hg38UCSC Ensembl
Innerchr4:103382434..103384860hg19UCSC Ensembl
Innerchr4:103601458..103603884hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382427
hg192427
hg182427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2329396, nssv2329399, nssv2329397, nssv2329398, nssv2329393, nssv2329390, nssv2329391, nssv2329395, nssv2329394, nssv2329392
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)nsv966302
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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