A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328358



Internal ID20861506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26836001..26837400hg38UCSC Ensembl
chr1:27162492..27163891hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060616
Samples
Known GenesZDHHC18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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