A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340542



Internal ID20998095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:192994865..193271149hg38UCSC Ensembl
chr2:193859591..194135874hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38276285
hg19276284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4237n223
Supporting Variantsnssv18081205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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