A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993137



Internal ID20560177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61340327..61340652hg38UCSC Ensembl
chr11:61107799..61108124hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466136
Supporting Variants
Samples
Known GenesDAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.98211


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