A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350801



Internal ID22576470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56725760..56944763hg38UCSC Ensembl
chr11:56493236..56712238hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38219004
hg19219003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908337
Supporting Variants
Samples
Known GenesMIR6128, OR9G4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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