A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009927



Internal ID19099146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85448516..85620005hg38UCSC Ensembl
Innerchr3:85497666..85669155hg19UCSC Ensembl
Innerchr3:85580356..85751845hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38171490
hg19171490
hg18171490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596268, nssv3596270, nssv3596269
Samples
Known GenesCADM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009927
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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