A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382601



Internal ID21040154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38597809..38803172hg38UCSC Ensembl
chr5:38597911..38803274hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38205364
hg19205364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213449
Samples
Known GenesLIFR-AS1, LOC101926904
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382601
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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