A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336155



Internal ID20993708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31955646..31961388hg38UCSC Ensembl
chr2:32180715..32186457hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg385743
hg195743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085288
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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