A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354305



Internal ID21011858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39177763..39207730hg38UCSC Ensembl
chr2:39404904..39434871hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3829968
hg1929968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086423
Samples
Known GenesCDKL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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