A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037233



Internal ID20604273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63277022..63277474hg38UCSC Ensembl
chr17:61354383..61354835hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525502
Supporting Variants
Samples
Known GenesTANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00235


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