A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713296



Internal ID19011577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105633807..105691858hg38UCSC Ensembl
Innerchr13:106286156..106344207hg19UCSC Ensembl
Innerchr13:105084157..105142208hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3858052
hg1958052
hg1858052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050333
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)nssv3713296
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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