A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037479



Internal ID20604519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68253359..68259519hg38UCSC Ensembl
chr17:66249500..66255660hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg386161
hg196161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520479
Supporting Variants
Samples
Known GenesAMZ2, ARSG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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