A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003005



Internal ID21912348
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 StatusM
Merged Variants
Supporting Variantsnssv17589162
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003005
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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