A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437896



Internal ID21095449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96625076..96625643hg38UCSC Ensembl
chr10:98384833..98385400hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985940
Samples
Known GenesPIK3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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