A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442497



Internal ID22500367
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 StatusS
Merged Variantsnsv5916960
Supporting Variants
Samples
Known GenesADAMTSL1, FAM154A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442497
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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