A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323688



Internal ID20856808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85611835..85647675hg38UCSC Ensembl
chr1:86077518..86113358hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3835841
hg1935841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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