A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972424



Internal ID18260954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95122524..95124643hg38UCSC Ensembl
Innerchr9:97884806..97886925hg19UCSC Ensembl
Innerchr9:96924627..96926746hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382120
hg192120
hg182120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559401, nssv2559402, nssv2559400, nssv2559399, nssv2559403, nssv2559395, nssv2559398, nssv2559396, nssv2559397, nssv2559404
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)nsv972424
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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