A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350073



Internal ID21007626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68482901..68487800hg38UCSC Ensembl
chr2:68710033..68714932hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088835
Samples
Known GenesAPLF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350073
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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