A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352240



Internal ID22577909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120982638..120986016hg38UCSC Ensembl
chr10:122742151..122745529hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg383379
hg193379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916038
Supporting Variants
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352240
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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