A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454539



Internal ID21112092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24268604..24373407hg38UCSC Ensembl
chr10:24557533..24662336hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38104804
hg19104804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979247
Samples
Known GenesKIAA1217, MIR603
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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