A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464263



Internal ID21121816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64979255..64991297hg38UCSC Ensembl
chr11:64746727..64758769hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3812043
hg1912043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994077
Samples
Known GenesBATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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