A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438791



Internal ID21096344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13424475..13425216hg38UCSC Ensembl
chr11:13446022..13446763hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988243
Samples
Known GenesBTBD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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