A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340765



Internal ID20998318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43411426..43438872hg38UCSC Ensembl
chr2:43638565..43666011hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3827447
hg1927447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088562
Samples
Known GenesTHADA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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