A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450131



Internal ID22508001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61000427..61005695hg38UCSC Ensembl
chr11:60767899..60773167hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg385269
hg195269
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863038
Supporting Variants
Samples
Known GenesCD6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450131
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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