A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349721



Internal ID21007274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55143002..55227567hg38UCSC Ensembl
chr2:55370138..55454703hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3884566
hg1984566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087571
Samples
Known GenesCLHC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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