A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397104



Internal ID21054657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126242420..126344460hg38UCSC Ensembl
chr5:125578113..125680152hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38102041
hg19102040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213177
Samples
Known GenesLOC101927488
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397104
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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