A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916960



Internal ID22692179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18908595..18962355hg38UCSC Ensembl
chr9:18908593..18962353hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3853761
hg1953761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442497
Samples
Known GenesADAMTSL1, FAM154A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916960
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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