A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606658



Internal ID20979729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142363401..142364200hg38UCSC Ensembl
chr6:142684538..142685337hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140146
Samples
Known GenesGPR126
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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