A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340295



Internal ID20997848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:49376830..49454961hg38UCSC Ensembl
chr2:49603969..49682099hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3878132
hg1978131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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