A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969409



Internal ID18257950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57939920..58071750hg38UCSC Ensembl
Innerchr6:58266198..58398028hg19UCSC Ensembl
Innerchr6:58374157..58505987hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38131831
hg19131831
hg18131831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2410666, nssv2410668, nssv2410663, nssv2410669, nssv2410665, nssv2410672, nssv2410670, nssv2410664, nssv2410667, nssv2410671
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGUSBP4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969409
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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