A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524752



Internal ID18823033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:84476359..84499950hg38UCSC Ensembl
Innerchr12:84870138..84893729hg19UCSC Ensembl
Innerchr12:83394269..83417860hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3823592
hg1923592
hg1823592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054448
Supporting Variants
Samples
Known GenesMIR548T
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524752
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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