A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761628



Internal ID22096124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58050631..58051631hg38UCSC Ensembl
chr11:57818103..57819103hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4441319
Supporting Variants
Samples
Known GenesOR9Q1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761628
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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