A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168901



Internal ID20735941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37742896..37747790hg38UCSC Ensembl
chr8:37600414..37605308hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg384895
hg194895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432376
Supporting Variants
Samples
Known GenesERLIN2, LOC728024
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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