A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342153



Internal ID20999706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203954901..203957300hg38UCSC Ensembl
chr2:204819624..204822023hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084965
Samples
Known GenesICOS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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