A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142936



Internal ID20709976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6297001..6300300hg38UCSC Ensembl
chr6:6297234..6300533hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397309
Supporting Variants
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00908


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