A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525578



Internal ID301734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51615723..51617903hg38UCSC Ensembl
chr17:49693084..49695264hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525578
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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