A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051653



Internal ID19140872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89149948..89185637hg38UCSC Ensembl
Innerchr13:89802202..89837891hg19UCSC Ensembl
Innerchr13:88600203..88635892hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3835690
hg1935690
hg1835690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1726n100
Supporting Variantsnssv3525458
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)nsv1051653
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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