A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334755



Internal ID20867943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40543754..40546838hg38UCSC Ensembl
chr1:41009426..41012510hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060760
Samples
Known GenesZNF684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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