A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460439



Internal ID21117992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44558709..44571135hg38UCSC Ensembl
chr11:44580259..44592685hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3812427
hg1912427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991666
Samples
Known GenesCD82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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