A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114632



Internal ID21477531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64968563..64971869hg38UCSC Ensembl
chr2:65195697..65199003hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383307
hg193307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572634
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114632
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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