A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035895



Internal ID19125114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:45866512..45889716hg38UCSC Ensembl
Innerchr13:46440647..46463851hg19UCSC Ensembl
Innerchr13:45338648..45361852hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3823205
hg1923205
hg1823205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523427
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)nsv1035895
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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