A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436691



Internal ID22494561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5233642..5244664hg38UCSC Ensembl
chr9:5233642..5244664hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3811023
hg1911023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914606
Supporting Variants
Samples
Known GenesINSL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436691
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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