A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3708151



Internal ID19006432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7851817..7970629hg38UCSC Ensembl
Innerchr12:8004413..8123225hg19UCSC Ensembl
Innerchr12:7895680..8014492hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38118813
hg19118813
hg18118813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053928
Supporting Variants
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3708151
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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