A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050042



Internal ID19139261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105633807..105695924hg38UCSC Ensembl
Innerchr13:106286156..106348273hg19UCSC Ensembl
Innerchr13:105084157..105146274hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3862118
hg1962118
hg1862118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1739n100
Supporting Variantsnssv3525566, nssv3525567
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)nsv1050042
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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