A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040521



Internal ID19129740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90004682..90043482hg38UCSC Ensembl
Innerchr13:90656936..90695736hg19UCSC Ensembl
Innerchr13:89454937..89493737hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3838801
hg1938801
hg1838801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1727n100
Supporting Variantsnssv3525472
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)nsv1040521
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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