A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114059



Internal ID21411707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3671554..3671709hg38UCSC Ensembl
chr2:3719144..3719299hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577531
Supporting Variants
SamplesHG00513
Known GenesALLC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114059
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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