A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577579



Internal ID21526033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218779934..218780159hg38UCSC Ensembl
chr2:219644657..219644882hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111442
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577579
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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