A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389181



Internal ID21046734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10429509..10543017hg38UCSC Ensembl
chr5:10429621..10543129hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38113509
hg19113509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212626
Samples
Known GenesLOC101929412, MARCH6, MIR6131, ROPN1L, ROPN1L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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