A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419556



Internal ID22477426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53798512..53809315hg38UCSC Ensembl
chr5:53094342..53105145hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3810804
hg1910804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906312
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419556
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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