A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468337



Internal ID22526226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76076258..76078732hg38UCSC Ensembl
chr10:77836016..77838490hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863024
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468337
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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