A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166852



Internal ID20733892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40640631..40641158hg38UCSC Ensembl
chr8:40498150..40498677hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432594
Supporting Variants
Samples
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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