A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444509



Internal ID21102062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48442900..48453815hg38UCSC Ensembl
chr10:49650943..49661858hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3810916
hg1910916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979984
Samples
Known GenesARHGAP22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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