A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335630



Internal ID20993183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46740672..46751806hg38UCSC Ensembl
chr2:46967811..46978945hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3811135
hg1911135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090580
Samples
Known GenesSOCS5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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