A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371038



Internal ID21028591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4634409..4663415hg38UCSC Ensembl
chr4:4636136..4665142hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3829007
hg1929007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213701
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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