A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703902



Internal ID21376178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111310365..111310657hg38UCSC Ensembl
chr6:111631568..111631860hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392590
Supporting Variants
Samples
Known GenesREV3L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703902
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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