A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459628



Internal ID21117181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59175548..59176744hg38UCSC Ensembl
chr11:58943021..58944217hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992007
Samples
Known GenesDTX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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