A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913392



Internal ID22688608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5901998..5903496hg38UCSC Ensembl
chr9:5901998..5903496hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441947
Samples
Known GenesMLANA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913392
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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