A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338726



Internal ID20996279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208894080..208905380hg38UCSC Ensembl
chr2:209758804..209770104hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3811301
hg1911301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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