A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110939



Internal ID18918751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37787643..37808996hg38UCSC Ensembl
Outerchr20:36416045..36437398hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3821354
hg1921354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961361
SamplesKWS1
Known GenesCTNNBL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110939
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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