A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437782



Internal ID21095335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24641774..24642427hg38UCSC Ensembl
chr10:24930703..24931356hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979258
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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