A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036656



Internal ID20603696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53805001..53806100hg38UCSC Ensembl
chr17:51882362..51883461hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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