A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468751



Internal ID22526640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61438889..61440188hg38UCSC Ensembl
chr11:61206361..61207660hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850067
Supporting Variants
Samples
Known GenesSDHAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468751
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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