A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349670



Internal ID21007223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70330338..70333025hg38UCSC Ensembl
chr2:70557470..70560157hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg382688
hg192688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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