A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965725



Internal ID18600955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53233522..53236518hg38UCSC Ensembl
Innerchr6:53098320..53101316hg19UCSC Ensembl
Innerchr6:53206279..53209275hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg382997
hg192997
hg182997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2410312, nssv2410316, nssv2410317, nssv2410320, nssv2410318, nssv2410319, nssv2410315, nssv2410321, nssv2410313, nssv2410314
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)nsv965725
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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