A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028265



Internal ID20595305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10296842..10331946hg38UCSC Ensembl
chr16:10390699..10425803hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3835105
hg1935105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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