A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335887



Internal ID20993440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176475251..176812364hg38UCSC Ensembl
chr2:177339979..177677092hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38337114
hg19337114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082055
Samples
Known GenesLINC01116, MIR1246
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335887
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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