A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350818



Internal ID21008371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64542212..64542823hg38UCSC Ensembl
chr2:64769346..64769957hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089311
Samples
Known GenesAFTPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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