A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052214



Internal ID19141433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86630897..86776017hg38UCSC Ensembl
Innerchr13:87283152..87428272hg19UCSC Ensembl
Innerchr13:86081153..86226273hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38145121
hg19145121
hg18145121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525437
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)nsv1052214
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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