A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349625



Internal ID21007178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176830447..176831085hg38UCSC Ensembl
chr2:177695175..177695813hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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