A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735248



Internal ID19033529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108833482..108909071hg38UCSC Ensembl
Innerchr3:108552329..108627918hg19UCSC Ensembl
Innerchr3:110035019..110110608hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3875590
hg1975590
hg1875590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007841
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)nssv3735248
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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