A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350224



Internal ID22575893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76315756..76316424hg38UCSC Ensembl
chr10:78075514..78076182hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909940
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350224
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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