A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110013



Internal ID21489479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21001069..21001203hg38UCSC Ensembl
chr2:21223941..21224075hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566618
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110013
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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