A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525325



Internal ID301490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31962975..31963740hg38UCSC Ensembl
chr17:30289994..30290759hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712615
Samples
Known GenesSUZ12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525325
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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