A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522880



Internal ID299136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34993212..34994148hg38UCSC Ensembl
chr17:33320231..33321167hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38937
hg19937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712787
Samples
Known GenesLIG3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522880
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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