A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035252



Internal ID19124471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:83649555..84052653hg38UCSC Ensembl
Innerchr12:84043334..84446432hg19UCSC Ensembl
Innerchr12:82567465..82970563hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38403099
hg19403099
hg18403099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1536n100
Supporting Variantsnssv3524747
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)nsv1035252
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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