A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888009



Internal ID22663009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7238110..7240131hg38UCSC Ensembl
chr5:7238223..7240244hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888009
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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