A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352781



Internal ID21010334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175628904..175637123hg38UCSC Ensembl
chr2:176493632..176501851hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg388220
hg198220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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