A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589162



Internal ID21781205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76045247..76045332hg38UCSC Ensembl
chr10:77805005..77805090hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003005
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589162
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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