A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338897



Internal ID20996450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223274998..223309012hg38UCSC Ensembl
chr2:224139716..224173730hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3834015
hg1934015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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