A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336726



Internal ID20994279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142677036..142677374hg38UCSC Ensembl
chr2:143434605..143434943hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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