A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410740



Internal ID22468610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40203704..40203760hg38UCSC Ensembl
chr4:40205324..40205380hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901123
Supporting Variants
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410740
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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