A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475314



Internal ID22533209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36916407..36918950hg38UCSC Ensembl
chr19:37407309..37409852hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382544
hg192544
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880820
Supporting Variants
Samples
Known GenesZNF568
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475314
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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