A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143842



Internal ID20710882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68736780..68737235hg38UCSC Ensembl
chr6:69446672..69447127hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400614
Supporting Variants
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00048


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