A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353728



Internal ID21011281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10310326..10326076hg38UCSC Ensembl
chr2:10450452..10466202hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3815751
hg1915751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205788
Samples
Known GenesHPCAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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