A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029155



Internal ID20596195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30417201..30418300hg38UCSC Ensembl
chr16:30428522..30429621hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506141
Supporting Variants
Samples
Known GenesZNF771
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01758


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