A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145649



Internal ID20712689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6492747..6493113hg38UCSC Ensembl
chr6:6492980..6493346hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399399
Supporting Variants
Samples
Known GenesLY86-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00068


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