A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338532



Internal ID20996085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201969182..201971270hg38UCSC Ensembl
chr2:202833905..202835993hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg382089
hg192089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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