A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340439



Internal ID20997992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189667484..189671052hg38UCSC Ensembl
chr2:190532210..190535778hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg383569
hg193569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083538
Samples
Known GenesASNSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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