A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135670



Internal ID20702710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9662497..9662970hg38UCSC Ensembl
chr5:9662609..9663082hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380701
Supporting Variants
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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