A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142998



Internal ID20710038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6385635..6398897hg38UCSC Ensembl
chr6:6385868..6399130hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3813263
hg1913263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400882
Supporting Variants
Samples
Known GenesLY86-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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