A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144808



Internal ID20711848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57161801..57163400hg38UCSC Ensembl
chr6:57026599..57028198hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411852
Supporting Variants
Samples
Known GenesZNF451
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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