A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403218



Internal ID21060771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28101328..28134175hg38UCSC Ensembl
chr6:28069106..28101953hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3832848
hg1932848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140857
Samples
Known GenesZSCAN16, ZSCAN16-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403218
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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