A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439437



Internal ID22497307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54954623..54958000hg38UCSC Ensembl
chr8:55867183..55870560hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg383378
hg193378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439437
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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