A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337943



Internal ID20995496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:147449801..147476100hg38UCSC Ensembl
chr2:148207369..148233668hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3826300
hg1926300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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