A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354316



Internal ID21011869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27373829..27375386hg38UCSC Ensembl
chr2:27596696..27598253hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381558
hg191558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085699
Samples
Known GenesSNX17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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