A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350444



Internal ID21007997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11813166..11822831hg38UCSC Ensembl
chr2:11953292..11962957hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg389666
hg199666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075455
Samples
Known GenesLPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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