A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338303



Internal ID20995856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163260001..163261000hg38UCSC Ensembl
chr2:164116511..164117510hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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