A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917603



Internal ID22692822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126024012..126024239hg38UCSC Ensembl
chr9:128786291..128786518hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917603
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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