A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450361



Internal ID21107914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97754692..97758165hg38UCSC Ensembl
chr10:99514449..99517922hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg383474
hg193474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985765
Samples
Known GenesZFYVE27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450361
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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