A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994185



Internal ID20561225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78183396..78195567hg38UCSC Ensembl
chr11:77894442..77906613hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3812172
hg1912172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471715
Supporting Variants
Samples
Known GenesKCTD21, USP35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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