A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354221



Internal ID21011774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79052050..79062314hg38UCSC Ensembl
chr2:79279176..79289440hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3810265
hg1910265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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