A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524836



Internal ID18476431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:97602456..97803043hg38UCSC Ensembl
Innerchr12:97996234..98196821hg19UCSC Ensembl
Innerchr12:96520365..96720952hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38200588
hg19200588
hg18200588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044240
Supporting Variants
Samples
Known GenesLOC643711
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524836
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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