A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339324



Internal ID20996877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28231682..28366249hg38UCSC Ensembl
chr2:28454549..28589116hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38134568
hg19134568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087493
Samples
Known GenesBRE, LOC100505716
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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