A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464142



Internal ID21121695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106092442..106093178hg38UCSC Ensembl
chr11:105963169..105963905hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986252
Samples
Known GenesAASDHPPT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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