A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578967



Internal ID21527442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234351232..234352846hg38UCSC Ensembl
chr2:235259876..235261490hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110243
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578967
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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