A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495932



Internal ID22553865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54141273..54146973hg38UCSC Ensembl
chr4:55007440..55013140hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839678
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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