A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138802



Internal ID337986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40000..107150hg38UCSC Ensembl
chr1:40000..107150hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3867151
hg1967151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900445
Samples
Known GenesOR4F5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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