A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475343



Internal ID22533238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37463204..37466329hg38UCSC Ensembl
chr19:37954106..37957231hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383126
hg193126
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883181
Supporting Variants
Samples
Known GenesZNF569
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475343
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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