A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401307



Internal ID21058860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1653120..1661817hg38UCSC Ensembl
chr6:1653354..1662051hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg388698
hg198698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217025
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401307
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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