A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992601



Internal ID20559641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66942136..66943476hg38UCSC Ensembl
chr11:66709607..66710947hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381341
hg191341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469840
Supporting Variants
Samples
Known GenesPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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