A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527266



Internal ID303368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63614883..63615327hg38UCSC Ensembl
chr17:61692243..61692687hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527266
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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