A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410513



Internal ID21068066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96804638..97148409hg38UCSC Ensembl
chr5:96140341..96484113hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38343772
hg19343773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215438
Samples
Known GenesERAP1, ERAP2, LIX1, LNPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410513
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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