A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474434



Internal ID21131987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58597501..58599000hg38UCSC Ensembl
chr11:58364974..58366473hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993754
Samples
Known GenesZFP91, ZFP91-CNTF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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