A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320987



Internal ID20854088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26304613..26312522hg38UCSC Ensembl
chr1:26631104..26639013hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387910
hg197910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060579
Samples
Known GenesUBXN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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