A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713292



Internal ID19011573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103596790..103625669hg38UCSC Ensembl
Innerchr13:104249140..104278019hg19UCSC Ensembl
Innerchr13:103047141..103076020hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3828880
hg1928880
hg1828880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053244
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)nssv3713292
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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