A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724898



Internal ID148564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60550986..60551296hg38UCSC Ensembl
chr17:58628347..58628657hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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