A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895648



Internal ID22670733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7395696..7395748hg38UCSC Ensembl
chr5:7395809..7395861hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895648
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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