A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337393



Internal ID20994946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75136244..75149578hg38UCSC Ensembl
chr2:75363370..75376704hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3813335
hg1913335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090244
Samples
Known GenesTACR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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