A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417566



Internal ID22475436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163165066..163166222hg38UCSC Ensembl
chr4:164086218..164087374hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895157
Supporting Variants
Samples
Known GenesNAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417566
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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