A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340331



Internal ID20997884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100582542..100590816hg38UCSC Ensembl
chr2:101199004..101207278hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg388275
hg198275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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