A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330776



Internal ID20863934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51264303..51266284hg38UCSC Ensembl
chr1:51729975..51731956hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381982
hg191982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061978
Samples
Known GenesRNF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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