A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439866



Internal ID22497736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99024276..99024276hg38UCSC Ensembl
chr9:101786558..101786558hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961196
Supporting Variants
Samples
Known GenesCOL15A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439866
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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