A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110247



Internal ID21503977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235375924..235375973hg38UCSC Ensembl
chr2:236284568..236284617hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579181
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110247
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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