A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862674



Internal ID22637609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128637693..128640292hg38UCSC Ensembl
chr9:131399972..131402571hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511446
Samples
Known GenesWDR34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862674
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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