A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041756



Internal ID21951086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62986797..62986797hg38UCSC Ensembl
chr2:63213932..63213932hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525605
Samples
Known GenesEHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041756
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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