A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993212



Internal ID20560252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62526480..62526899hg38UCSC Ensembl
chr11:62293952..62294371hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457176
Supporting Variants
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0009


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