A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490696



Internal ID22548620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158187684..158193653hg38UCSC Ensembl
chr4:159108836..159114805hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385970
hg195970
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838323
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490696
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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