A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367109



Internal ID22592778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76076060..76078551hg38UCSC Ensembl
chr10:77835818..77838309hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382492
hg192492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926308
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367109
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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