A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450695



Internal ID21108248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96344562..96345024hg38UCSC Ensembl
chr10:98104319..98104781hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985922
Samples
Known GenesOPALIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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