A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032713



Internal ID20599753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75396355..75428854hg38UCSC Ensembl
chr16:75430253..75462752hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3832500
hg1932500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513157
Supporting Variants
Samples
Known GenesCFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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