A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328356



Internal ID20861503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54064658..54075611hg38UCSC Ensembl
chr1:54530331..54541284hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3810954
hg1910954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061532
Samples
Known GenesTCEANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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