A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994689



Internal ID20561729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84829926..84890879hg38UCSC Ensembl
chr11:84540969..84601923hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3860954
hg1960955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464743
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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