A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992674



Internal ID20559714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61011889..61018693hg38UCSC Ensembl
chr11:60779361..60786165hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg386805
hg196805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464939
Supporting Variants
Samples
Known GenesCD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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