A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494466



Internal ID22552397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36174522..36176755hg38UCSC Ensembl
chr4:36176144..36178377hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839564
Supporting Variants
Samples
Known GenesARAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494466
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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