A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018636



Internal ID19107853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2921825..3002862hg38UCSC Ensembl
Innerchr9:2921825..3002862hg19UCSC Ensembl
Innerchr9:2911825..2992862hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3881038
hg1981038
hg1881038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758086
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)nsv1018636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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