A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338588



Internal ID20996141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180506600..180507218hg38UCSC Ensembl
chr2:181371327..181371945hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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