A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905647



Internal ID22680836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177254873..177256567hg38UCSC Ensembl
chr4:178176027..178177721hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905647
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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