A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527193



Internal ID303298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62830313..62831074hg38UCSC Ensembl
chr17:60907674..60908435hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713958
Samples
Known GenesMIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527193
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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