A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897733



Internal ID22672839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36610617..36610677hg38UCSC Ensembl
chr5:36610719..36610779hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410778
Samples
Known GenesSLC1A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897733
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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