A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352696



Internal ID21010249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:133949559..133991014hg38UCSC Ensembl
chr2:134707130..134748585hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3841456
hg1941456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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