A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212397



Internal ID20779437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77968002..78733677hg38UCSC Ensembl
chr4:78889156..79654831hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38765676
hg19765676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380868
Supporting Variants
Samples
Known GenesANXA3, FRAS1, LINC01094
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212397
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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