A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354439



Internal ID21011992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210721034..210769457hg38UCSC Ensembl
chr2:211585758..211634181hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3848424
hg1948424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084707
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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