A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409705



Internal ID22467575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53488433..53488508hg38UCSC Ensembl
chr5:52784263..52784338hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409705
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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