A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444385



Internal ID21101938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6720630..6721802hg38UCSC Ensembl
chr11:6741861..6743033hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993477
Samples
Known GenesGVINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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