A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726002



Internal ID19024283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46424485..46448526hg38UCSC Ensembl
Innerchr2:46651624..46675665hg19UCSC Ensembl
Innerchr2:46505128..46529169hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3824042
hg1924042
hg1824042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001902
Supporting Variants
Samples
Known GenesLOC101805491
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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