A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045733



Internal ID19134952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50613439..50643328hg38UCSC Ensembl
Innerchr13:51187575..51217464hg19UCSC Ensembl
Innerchr13:50085576..50115465hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3829890
hg1929890
hg1829890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523460
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)nsv1045733
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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