A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039069



Internal ID20606109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78009804..78010126hg38UCSC Ensembl
chr17:76005885..76006207hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516998
Supporting Variants
Samples
Known GenesTNRC6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00295


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