A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437294



Internal ID21094847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18187301..18192000hg38UCSC Ensembl
chr11:18208848..18213547hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv978n223
Supporting Variantsnssv18192814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437294
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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