A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046376



Internal ID19135595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54210901..54253666hg38UCSC Ensembl
Innerchr13:54785036..54827801hg19UCSC Ensembl
Innerchr13:53683037..53725802hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3842766
hg1942766
hg1842766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523480
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)nsv1046376
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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