A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711841



Internal ID19010122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68585591..68627101hg38UCSC Ensembl
Innerchr13:69159723..69201233hg19UCSC Ensembl
Innerchr13:68057724..68099234hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3841511
hg1941511
hg1841511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050299
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)nssv3711841
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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