A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524636



Internal ID18822917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:74205883..74293883hg38UCSC Ensembl
Innerchr12:74599663..74687663hg19UCSC Ensembl
Innerchr12:72885930..72973930hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3888001
hg1988001
hg1888001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047574
Supporting Variants
Samples
Known GenesLOC100507377
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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