A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438104



Internal ID21095657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30703733..30704362hg38UCSC Ensembl
chr11:30725280..30725909hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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