A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900624



Internal ID22675767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183642190..183642364hg38UCSC Ensembl
chr4:184563343..184563517hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417283
Samples
Known GenesRWDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900624
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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