A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968747



Internal ID18603975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109532666..109535007hg38UCSC Ensembl
Innerchr9:112294946..112297287hg19UCSC Ensembl
Innerchr9:111334767..111337108hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg382342
hg192342
hg182342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2562153, nssv2562152, nssv2562149, nssv2562148, nssv2562157, nssv2562151, nssv2562155, nssv2562156, nssv2562150, nssv2562154
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968747
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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