A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992559



Internal ID20559599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66244401..66252715hg38UCSC Ensembl
chr11:66011872..66020186hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg388315
hg198315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467961
Supporting Variants
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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