A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001124



Internal ID19090341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85117897..85259896hg38UCSC Ensembl
Innerchr3:85167047..85309046hg19UCSC Ensembl
Innerchr3:85249737..85391736hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38142000
hg19142000
hg18142000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596267
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)nsv1001124
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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