A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441140



Internal ID21098693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96646539..96647139hg38UCSC Ensembl
chr10:98406296..98406896hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985944
Samples
Known GenesPIK3AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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