A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403665



Internal ID21061218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62555628..62865520hg38UCSC Ensembl
chr5:61851455..62161347hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38309893
hg19309893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216272
Samples
Known GenesIPO11, IPO11-LRRC70, LRRC70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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