A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033666



Internal ID20600706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87755841..87773212hg38UCSC Ensembl
chr16:87789447..87806818hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3817372
hg1917372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509643
Supporting Variants
Samples
Known GenesKLHDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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