A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169001



Internal ID20736041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39072616..39202220hg38UCSC Ensembl
chr8:38930135..39059739hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38129605
hg19129605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423142
Supporting Variants
Samples
Known GenesADAM32, ADAM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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