A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735246



Internal ID19033527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108832182..108939054hg38UCSC Ensembl
Innerchr3:108551029..108657901hg19UCSC Ensembl
Innerchr3:110033719..110140591hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38106873
hg19106873
hg18106873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999583
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)nssv3735246
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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