A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567656



Internal ID21515994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10331920..10331981hg38UCSC Ensembl
chr2:10472046..10472107hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107249
SamplesHG03125
Known GenesHPCAL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567656
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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