A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407614



Internal ID22465484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38598068..38598233hg38UCSC Ensembl
chr19:39088708..39088873hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931671
Supporting Variants
Samples
Known GenesMAP4K1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407614
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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