A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039143



Internal ID20606183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9450364..9458391hg38UCSC Ensembl
chr17:9353681..9361708hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg388028
hg198028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513397
Supporting Variants
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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