A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036901



Internal ID20603941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55081901..55082700hg38UCSC Ensembl
chr17:53159262..53160061hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520462
Supporting Variants
Samples
Known GenesSTXBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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