A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037592



Internal ID20604633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69102601..69103300hg38UCSC Ensembl
chr17:67098742..67099441hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532194
Supporting Variants
Samples
Known GenesABCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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