A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411860



Internal ID22469730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15755733..15756176hg38UCSC Ensembl
chr4:15757356..15757799hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411860
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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