A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464953



Internal ID22522841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34135927..34137026hg38UCSC Ensembl
chr11:34157474..34158573hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865991
Supporting Variants
Samples
Known GenesNAT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464953
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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