A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992404



Internal ID20559444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56149374..56499735hg38UCSC Ensembl
chr11:55916850..56267211hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38350362
hg19350362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475397
Supporting Variants
Samples
Known GenesOR5J2, OR5M3, OR5M8, OR5M9, OR5R1, OR5T1, OR5T2, OR5T3, OR8H1, OR8J1, OR8K1, OR8K3, OR8K5, OR8U1, OR8U8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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