A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398806



Internal ID21056359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2165855..2585137hg38UCSC Ensembl
chr6:2166089..2585371hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38419283
hg19419283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222981
Samples
Known GenesGMDS, GMDS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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