A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002823



Internal ID18745355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:23236347..23581592hg38UCSC Ensembl
Innerchr3:23277838..23623083hg19UCSC Ensembl
Innerchr3:23252842..23598087hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38345246
hg19345246
hg18345246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739653
Samples
Known GenesMIR548AC, UBE2E2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002823
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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