A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040236



Internal ID19129455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53354060..53380925hg38UCSC Ensembl
Innerchr13:53928195..53955060hg19UCSC Ensembl
Innerchr13:52826196..52853061hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3826866
hg1926866
hg1826866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1654n100
Supporting Variantsnssv3523475
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)nsv1040236
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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