A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349448



Internal ID21007001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222110596..222110975hg38UCSC Ensembl
chr2:222975315..222975694hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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