A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400034



Internal ID21057587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46127901..46133100hg38UCSC Ensembl
chr6:46095638..46100837hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231895
Samples
Known GenesENPP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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