A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451021



Internal ID22508894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7420773..7429185hg38UCSC Ensembl
chr11:7442004..7450416hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388413
hg198413
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854925
Supporting Variants
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451021
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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