A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448906



Internal ID21106459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27542395..27543869hg38UCSC Ensembl
chr10:27831324..27832798hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381475
hg191475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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