A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033894



Internal ID20600934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15395328..15397749hg38UCSC Ensembl
chr17:15298645..15301066hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382422
hg192422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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