A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212535



Internal ID20779575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56381363..56384866hg38UCSC Ensembl
chr4:57247529..57251032hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383504
hg193504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388633
Supporting Variants
Samples
Known GenesAASDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212535
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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