A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338384



Internal ID20995937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203032201..203039100hg38UCSC Ensembl
chr2:203896924..203903823hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084361
Samples
Known GenesNBEAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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