A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724714



Internal ID148380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50512838..50512946hg38UCSC Ensembl
chr17:48590199..48590307hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521771
Supporting Variants
Samples
Known GenesMYCBPAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724714
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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