A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399764



Internal ID21057317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1757008..1759055hg38UCSC Ensembl
chr6:1757242..1759289hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143271
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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