A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524627



Internal ID18822908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73906179..74031669hg38UCSC Ensembl
Innerchr12:74299959..74425449hg19UCSC Ensembl
Innerchr12:72586226..72711716hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38125491
hg19125491
hg18125491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041875
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)nssv3524627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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