A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712494



Internal ID19010775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:63143632..63188553hg38UCSC Ensembl
Innerchr12:63537412..63582333hg19UCSC Ensembl
Innerchr12:61823679..61868600hg18UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg3844922
hg1944922
hg1844922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035231
Supporting Variants
Samples
Known GenesAVPR1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712494
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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