A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472927



Internal ID21130480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75497455..75498602hg38UCSC Ensembl
chr11:75208500..75209647hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993654
Samples
Known GenesGDPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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