A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449009



Internal ID21106562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110304401..110304800hg38UCSC Ensembl
chr10:112064159..112064558hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979499
Samples
Known GenesSMNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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