A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317933



Internal ID20851023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221521201..221727100hg38UCSC Ensembl
chr1:221694543..221900442hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38205900
hg19205900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058031
Samples
Known GenesDUSP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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