A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110989



Internal ID20678029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157235201..157236600hg38UCSC Ensembl
chr4:158156353..158157752hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384787
Supporting Variants
Samples
Known GenesGRIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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