A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524645



Internal ID18476240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:79649380..79684747hg38UCSC Ensembl
Innerchr12:80043160..80078527hg19UCSC Ensembl
Innerchr12:78567291..78602658hg18UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3835368
hg1935368
hg1835368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043290
Supporting Variants
Samples
Known GenesPAWR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524645
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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