A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595185



Internal ID21787228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41646910..41646975hg38UCSC Ensembl
chr8:41504429..41504494hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008366
Supporting Variants
Samples
Known GenesNKX6-3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595185
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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