A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965693



Internal ID18600923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26876493..26879412hg38UCSC Ensembl
Innerchr6:26844272..26847191hg19UCSC Ensembl
Innerchr6:26952251..26955170hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382920
hg192920
hg182920
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2705928, nssv2705929, nssv2705927, nssv2705923, nssv2705931, nssv2705924, nssv2705926, nssv2705930, nssv2705925, nssv2705932
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGUSBP2
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965693
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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