A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168900



Internal ID20735940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37737128..37738419hg38UCSC Ensembl
chr8:37594646..37595937hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424090
Supporting Variants
Samples
Known GenesERLIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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