A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137155



Internal ID21464763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107692953..107701195hg38UCSC Ensembl
chr3:107411800..107420042hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg388243
hg198243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566944
Supporting Variants
SamplesHG03065
Known GenesBBX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137155
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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