A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524799



Internal ID18823080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:87109480..87199022hg38UCSC Ensembl
Innerchr12:87503257..87592799hg19UCSC Ensembl
Innerchr12:86027388..86116930hg18UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg3889543
hg1989543
hg1889543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036043
Supporting Variants
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)nssv3524799
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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