A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452908



Internal ID21110461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15674961..15675509hg38UCSC Ensembl
chr10:15716960..15717508hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978784
Samples
Known GenesITGA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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