A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034620



Internal ID20601660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16550513..16551012hg38UCSC Ensembl
chr17:16453827..16454326hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503927
Supporting Variants
Samples
Known GenesZNF287
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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