A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409805



Internal ID21067358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52742568..52755447hg38UCSC Ensembl
chr6:52607366..52620245hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3812880
hg1912880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234923
Samples
Known GenesGSTA2, GSTA7P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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