A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447160



Internal ID21104713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4209901..4212200hg38UCSC Ensembl
chr10:4252093..4254392hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980163
Samples
Known GenesLINC00702
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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