A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706917



Internal ID21379193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200965425..200965835hg38UCSC Ensembl
chr2:201830148..201830558hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390132
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706917
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0114943


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