A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341789



Internal ID20999342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234655060..234663427hg38UCSC Ensembl
chr2:235563704..235572071hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg388368
hg198368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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