A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892057



Internal ID22667102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42972881..42973005hg38UCSC Ensembl
chr4:42974898..42975022hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410595
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892057
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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