A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383693



Internal ID21041246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48105354..48147744hg38UCSC Ensembl
chr4:48107371..48149761hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3842391
hg1942391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117267
Samples
Known GenesTEC, TXK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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