A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213596



Internal ID20780636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39897847..40109316hg38UCSC Ensembl
chr4:39899467..40110936hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38211470
hg19211470
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389941
Supporting Variants
Samples
Known GenesLOC344967, N4BP2, PDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213596
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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