A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972778



Internal ID18261308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92139786..92145991hg38UCSC Ensembl
Innerchr9:94902068..94908273hg19UCSC Ensembl
Innerchr9:93941889..93948094hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386206
hg196206
hg186206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557379, nssv2557374, nssv2557376, nssv2557373, nssv2557380, nssv2557377, nssv2557375, nssv2557372, nssv2557378, nssv2557371
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)nsv972778
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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