A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735245



Internal ID19033526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108801003..108920780hg38UCSC Ensembl
Innerchr3:108519850..108639627hg19UCSC Ensembl
Innerchr3:110002540..110122317hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38119778
hg19119778
hg18119778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014353
Supporting Variants
Samples
Known GenesGUCA1C, TRAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3735245
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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