A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764046



Internal ID18965279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22583661..22584862hg38UCSC Ensembl
chr20:22564299..22565500hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073050
Supporting Variants
SamplesKWP1
Known GenesFOXA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764046
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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