A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490177



Internal ID22548099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126434302..126436476hg38UCSC Ensembl
chr4:127355457..127357631hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490177
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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