A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993624



Internal ID20560664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74858781..74867112hg38UCSC Ensembl
chr11:74569826..74578157hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg388332
hg198332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464337
Supporting Variants
Samples
Known GenesXRRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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