A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925573



Internal ID22700800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92250608..92250676hg38UCSC Ensembl
chr9:95012890..95012958hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442342
Samples
Known GenesIARS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925573
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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