A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524897



Internal ID18476492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109323347..109368764hg38UCSC Ensembl
Innerchr12:109761152..109806569hg19UCSC Ensembl
Innerchr12:108245535..108290952hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3845418
hg1945418
hg1845418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044876
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)nssv3524897
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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