A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515046



Internal ID291533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74973553..74976452hg38UCSC Ensembl
chr17:72969648..72972547hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515046
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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