A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972779



Internal ID18261309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92148325..92157801hg38UCSC Ensembl
Innerchr9:94910607..94920083hg19UCSC Ensembl
Innerchr9:93950428..93959904hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg389477
hg199477
hg189477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557470, nssv2557471, nssv2557469, nssv2557468, nssv2557475, nssv2557477, nssv2557474, nssv2557476, nssv2557473, nssv2557472
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLINC00475
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972779
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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