A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979886



Internal ID18615087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143511747..143522597hg38UCSC Ensembl
Innerchr3:143230589..143241439hg19UCSC Ensembl
Innerchr3:144713279..144724129hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3810851
hg1910851
hg1810851
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2299179, nssv2299173, nssv2299171, nssv2299172, nssv2299178, nssv2299177, nssv2299180, nssv2299174, nssv2299176, nssv2299175
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSLC9A9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979886
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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