A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209521



Internal ID20776561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109726701..109729900hg38UCSC Ensembl
chr4:110647857..110651056hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387650
Supporting Variants
Samples
Known GenesPLA2G12A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209521
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00025


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