A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993144



Internal ID20560184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61431073..61459626hg38UCSC Ensembl
chr11:61198545..61227098hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3828554
hg1928554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472274
Supporting Variants
Samples
Known GenesSDHAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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