A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713300



Internal ID18664895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107200567..107404351hg38UCSC Ensembl
Innerchr13:107852915..108056699hg19UCSC Ensembl
Innerchr13:106650916..106854700hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38203785
hg19203785
hg18203785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050833
Supporting Variants
Samples
Known GenesFAM155A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713300
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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