A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468429



Internal ID21125982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57683191..57688135hg38UCSC Ensembl
chr11:57450663..57455607hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg384945
hg194945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993442
Samples
Known GenesZDHHC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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