A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405214



Internal ID21062767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96387085..97100180hg38UCSC Ensembl
chr5:95722789..96435884hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38713096
hg19713096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215434
Samples
Known GenesCAST, ERAP1, ERAP2, LIX1, LNPEP, PCSK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405214
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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