A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714929



Internal ID19013210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18600494..18737640hg38UCSC Ensembl
Innerchr13:19174634..19311780hg19UCSC Ensembl
Innerchr13:18072634..18209780hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38137147
hg19137147
hg18137147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042239
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)nssv3714929
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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