A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893139



Internal ID22668197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42631167..42631975hg38UCSC Ensembl
chr5:42631269..42632077hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426385
Samples
Known GenesGHR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893139
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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