A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416331



Internal ID22474201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56354413..56358190hg38UCSC Ensembl
chr5:55650240..55654017hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg383778
hg193778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416331
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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