A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166861



Internal ID20733901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40718197..40723803hg38UCSC Ensembl
chr8:40575716..40581322hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg385607
hg195607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422989
Supporting Variants
Samples
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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