A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349962



Internal ID21007515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55837484..55838947hg38UCSC Ensembl
chr2:56064619..56066082hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg381464
hg191464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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