A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471306



Internal ID21128859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78115223..78115574hg38UCSC Ensembl
chr11:77826269..77826620hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994177
Samples
Known GenesALG8, RNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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