A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356926



Internal ID22582595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75830461..75830602hg38UCSC Ensembl
chr10:77590219..77590360hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926159
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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