A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994329



Internal ID20561369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76586545..76728785hg38UCSC Ensembl
chr11:76297589..76439829hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38142241
hg19142241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466026
Supporting Variants
Samples
Known GenesGUCY2EP, LRRC32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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