A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907174



Internal ID22682379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158477557..158546124hg38UCSC Ensembl
chr4:159398709..159467276hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3868568
hg1968568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412786
Samples
Known GenesRXFP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907174
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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