A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995516



Internal ID20562556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94475497..94482697hg38UCSC Ensembl
chr11:94208663..94215863hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg387201
hg197201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458901
Supporting Variants
Samples
Known GenesMRE11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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