A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036417



Internal ID19125636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100715746..100747558hg38UCSC Ensembl
Innerchr9:103478028..103509840hg19UCSC Ensembl
Innerchr9:102517849..102549661hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3831813
hg1931813
hg1831813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759791
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036417
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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