A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354112



Internal ID21011665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16714401..16717300hg38UCSC Ensembl
chr2:16895668..16898567hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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