A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711766



Internal ID19010047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:59499093..59523605hg38UCSC Ensembl
Innerchr13:60073227..60097739hg19UCSC Ensembl
Innerchr13:58971228..58995740hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3824513
hg1924513
hg1824513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049150
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)nssv3711766
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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