A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354064



Internal ID21011617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69991569..70009399hg38UCSC Ensembl
chr2:70218701..70236531hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3817831
hg1917831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088911
Samples
Known GenesPCBP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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