A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523663



Internal ID18821944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:61751601..61783183hg38UCSC Ensembl
Innerchr12:62145382..62176964hg19UCSC Ensembl
Innerchr12:60431649..60463231hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3831583
hg1931583
hg1831583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040154
Supporting Variants
Samples
Known GenesFAM19A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523663
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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