A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524366



Internal ID300574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16409867..16411399hg38UCSC Ensembl
chr17:16313181..16314713hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524366
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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