A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981211



Internal ID18616410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170714481..170734690hg38UCSC Ensembl
Innerchr6:171023569..171043778hg19UCSC Ensembl
Innerchr6:170865494..170885703hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3820210
hg1920210
hg1820210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2433087, nssv2433088, nssv2433091, nssv2433093, nssv2433089, nssv2433094, nssv2433096, nssv2433095, nssv2433090, nssv2433092
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)nsv981211
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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