A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972425



Internal ID18260955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95185277..95185870hg38UCSC Ensembl
Innerchr9:97947559..97948152hg19UCSC Ensembl
Innerchr9:96987380..96987973hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38594
hg19594
hg18594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559497, nssv2559495, nssv2559493, nssv2559496, nssv2559498, nssv2559492, nssv2559501, nssv2559500, nssv2559494, nssv2559499
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFANCC
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972425
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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