A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037748



Internal ID20604788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64051801..64059800hg38UCSC Ensembl
chr17:62129161..62137160hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529544
Supporting Variants
Samples
Known GenesERN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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