A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037329



Internal ID19126548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65009601..65099524hg38UCSC Ensembl
Innerchr13:65583733..65673656hg19UCSC Ensembl
Innerchr13:64481734..64571657hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3889924
hg1989924
hg1889924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3527912
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)nsv1037329
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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