A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333531



Internal ID20866709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94903099..94903667hg38UCSC Ensembl
chr1:95368655..95369223hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066074
Samples
Known GenesCNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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