A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214412



Internal ID20781452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99312267..99367523hg38UCSC Ensembl
chr4:100233424..100288680hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3855257
hg1955257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380028
Supporting Variants
Samples
Known GenesADH1B, ADH1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214412
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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