A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467893



Internal ID22525783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106954362..106958495hg38UCSC Ensembl
chr11:106825088..106829221hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384134
hg194134
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856205
Supporting Variants
Samples
Known GenesGUCY1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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