A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523596



Internal ID18475191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:55313191..55326825hg38UCSC Ensembl
Innerchr12:55706975..55720609hg19UCSC Ensembl
Innerchr12:53993242..54006876hg18UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3813635
hg1913635
hg1813635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050720
Supporting Variants
Samples
Known GenesOR6C1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523596
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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