A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525534



Internal ID18823815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102046039..102106184hg38UCSC Ensembl
Innerchr13:102698389..102758534hg19UCSC Ensembl
Innerchr13:101496390..101556535hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3860146
hg1960146
hg1860146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039315
Supporting Variants
Samples
Known GenesFGF14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525534
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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