A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900762



Internal ID22675907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223940788..223940967hg38UCSC Ensembl
chr2:224805505..224805684hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400921
Samples
Known GenesWDFY1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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