A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524626



Internal ID18822907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73841341..73972968hg38UCSC Ensembl
Innerchr12:74235121..74366748hg19UCSC Ensembl
Innerchr12:72521388..72653015hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38131628
hg19131628
hg18131628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053658
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)nssv3524626
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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