A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994158



Internal ID20561198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77735928..77739045hg38UCSC Ensembl
chr11:77446973..77450090hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458271
Supporting Variants
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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