A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475486



Internal ID22533382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15701066..15719107hg38UCSC Ensembl
chr17:15604380..15622421hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3818042
hg1918042
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884398
Supporting Variants
Samples
Known GenesZNF286A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475486
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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