A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352482



Internal ID21010035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9288336..9300194hg38UCSC Ensembl
chr2:9428465..9440323hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3811859
hg1911859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092585
Samples
Known GenesASAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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