A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179771



Internal ID20746811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34619373..34767757hg38UCSC Ensembl
chr11:34640920..34789304hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38148385
hg19148385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459142
Supporting Variants
Samples
Known GenesEHF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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