A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474442



Internal ID21131995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125918774..125919877hg38UCSC Ensembl
chr11:125788669..125789772hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987318
Samples
Known GenesDDX25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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