A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972456



Internal ID18260986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130499927..130501236hg38UCSC Ensembl
Innerchr9:133375314..133376623hg19UCSC Ensembl
Innerchr9:132365135..132366444hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381310
hg191310
hg181310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2567194, nssv2567190, nssv2567197, nssv2567188, nssv2567191, nssv2567195, nssv2567193, nssv2567189, nssv2567196, nssv2567192
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesASS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972456
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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