A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525476



Internal ID18823757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90522064..90566882hg38UCSC Ensembl
Innerchr13:91174318..91219136hg19UCSC Ensembl
Innerchr13:89972319..90017137hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3844819
hg1944819
hg1844819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052041
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525476
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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