A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969691



Internal ID18604918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65719388..65737118hg38UCSC Ensembl
Innerchr9:70428927..70446657hg19UCSC Ensembl
Innerchr9:69668747..69686477hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3817731
hg1917731
hg1817731
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2748239, nssv2749236, nssv2751601, nssv2750008, nssv2755635, nssv2751137, nssv2751074, nssv2756012, nssv2756166, nssv2750603
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD3, CBWD5, FOXD4L2, FOXD4L4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969691
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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