A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050020



Internal ID19139239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85874902..85925538hg38UCSC Ensembl
Innerchr13:86449037..86499673hg19UCSC Ensembl
Innerchr13:85347038..85397674hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3850637
hg1950637
hg1850637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525420
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)nsv1050020
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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