A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054691



Internal ID19143910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84504145..84526843hg38UCSC Ensembl
Innerchr13:85078280..85100978hg19UCSC Ensembl
Innerchr13:83976281..83998979hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3822699
hg1922699
hg1822699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525412
Samples
Known GenesLINC00333
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054691
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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