A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116466



Internal ID19276996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:85316774..85343173hg38UCSC Ensembl
Outerchr2:85543897..85570296hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3826400
hg1926400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978647
SamplesKWS2
Known GenesRETSAT, TGOLN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116466
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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