A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398712



Internal ID21056265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36526749..36530029hg38UCSC Ensembl
chr6:36494526..36497806hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg383281
hg193281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141759
Samples
Known GenesSTK38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398712
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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