A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472049



Internal ID21129602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130896282..131017149hg38UCSC Ensembl
chr11:130766177..130887044hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38120868
hg19120868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988418
Samples
Known GenesSNX19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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