A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340978



Internal ID20998531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228714789..228919202hg38UCSC Ensembl
chr2:229579505..229783918hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38204414
hg19204414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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