A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448466



Internal ID21106019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70129584..70134347hg38UCSC Ensembl
chr10:71889340..71894103hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384764
hg194764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983520
Samples
Known GenesAIFM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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