A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335966



Internal ID20993519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138574371..138584504hg38UCSC Ensembl
chr2:139331941..139342074hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3810134
hg1910134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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