A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972791



Internal ID18608007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97245200..97275606hg38UCSC Ensembl
Innerchr9:100007482..100037888hg19UCSC Ensembl
Innerchr9:99047303..99077709hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3830407
hg1930407
hg1830407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563635, nssv2563641, nssv2563632, nssv2563636, nssv2563637, nssv2563640, nssv2563633, nssv2563639, nssv2563634, nssv2563638
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972791
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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