A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475488



Internal ID22533384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15719545..15729326hg38UCSC Ensembl
chr17:15622859..15632640hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg389782
hg199782
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877268
Supporting Variants
Samples
Known GenesZNF286A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475488
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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