A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921677



Internal ID22696901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135052345..135052415hg38UCSC Ensembl
chr9:137944191..137944261hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921677
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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