A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346862



Internal ID21004415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:153399385..153414280hg38UCSC Ensembl
chr2:154255899..154270794hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3814896
hg1914896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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