A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028697



Internal ID20595737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12406701..12408800hg38UCSC Ensembl
chr16:12500558..12502657hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514393
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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