A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524628



Internal ID18822909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73915755..74023142hg38UCSC Ensembl
Innerchr12:74309535..74416922hg19UCSC Ensembl
Innerchr12:72595802..72703189hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38107388
hg19107388
hg18107388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037477
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)nssv3524628
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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