A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091007



Internal ID22000240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32503810..32503810hg38UCSC Ensembl
chr11:32525356..32525356hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091007
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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