A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341640



Internal ID20999193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:147985489..148017147hg38UCSC Ensembl
chr2:148743058..148774716hg19UCSC Ensembl
Cytoband2q23.1
Allele length
AssemblyAllele length
hg3831659
hg1931659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078782
Samples
Known GenesORC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341640
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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