A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490249



Internal ID22548171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142922045..142933733hg38UCSC Ensembl
chr4:143843198..143854886hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3811689
hg1911689
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490249
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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