A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406697



Internal ID22464567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38313159..38314401hg38UCSC Ensembl
chr19:38803799..38805041hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381243
hg191243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933780
Supporting Variants
Samples
Known GenesYIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406697
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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