A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966998



Internal ID18602227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31180648..31182813hg38UCSC Ensembl
Innerchr3:31222140..31224305hg19UCSC Ensembl
Innerchr3:31197144..31199309hg18UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg382166
hg192166
hg182166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2276271, nssv2276268, nssv2276270, nssv2276269, nssv2276274, nssv2276266, nssv2276272, nssv2276273, nssv2276267, nssv2276265
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)nsv966998
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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