A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419033



Internal ID22476903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72529064..72529206hg38UCSC Ensembl
chr5:71824891..71825033hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419033
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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