A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967771



Internal ID18256313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86860245..86877360hg38UCSC Ensembl
Innerchr4:87781398..87798513hg19UCSC Ensembl
Innerchr4:88000422..88017537hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3817116
hg1917116
hg1817116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2327037, nssv2327036, nssv2327034, nssv2327041, nssv2327040, nssv2327038, nssv2327032, nssv2327039, nssv2327033, nssv2327035
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC4orf36
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967771
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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