A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969386



Internal ID18604613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33329888..33357339hg38UCSC Ensembl
Innerchr6:33297665..33325116hg19UCSC Ensembl
Innerchr6:33405643..33433094hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3827452
hg1927452
hg1827452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2405490, nssv2405486, nssv2405492, nssv2405489, nssv2405485, nssv2405491, nssv2405484, nssv2405493, nssv2405487, nssv2405488
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)nsv969386
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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