A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323843



Internal ID20856965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35846715..35851509hg38UCSC Ensembl
chr1:36312316..36317110hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg384795
hg194795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060711
Samples
Known GenesAGO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323843
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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