A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084938



Internal ID21994171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44309154..44309154hg38UCSC Ensembl
chr11:44330704..44330704hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582894
Samples
Known GenesALX4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084938
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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