A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045865



Internal ID19135084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83525987..83581865hg38UCSC Ensembl
Innerchr13:84100122..84156000hg19UCSC Ensembl
Innerchr13:82998123..83054001hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3855879
hg1955879
hg1855879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1718n100
Supporting Variantsnssv3530549, nssv3530548
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)nsv1045865
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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