A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912857



Internal ID22688073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7420813..7429219hg38UCSC Ensembl
chr11:7442044..7450450hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388407
hg198407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351875
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912857
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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