A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525573



Internal ID18823854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107514878..107528415hg38UCSC Ensembl
Innerchr13:108167226..108180763hg19UCSC Ensembl
Innerchr13:106965227..106978764hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3813538
hg1913538
hg1813538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051067
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)nssv3525573
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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