A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991122



Internal ID20558162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46948468..46949168hg38UCSC Ensembl
chr11:46970019..46970719hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472404
Supporting Variants
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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