A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572871



Internal ID21521265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85474550..85474607hg38UCSC Ensembl
chr2:85701673..85701730hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115617
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572871
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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