A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926604



Internal ID22701831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135238700..135250141hg38UCSC Ensembl
chr9:138130546..138141987hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3811442
hg1911442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926604
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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