A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140364



Internal ID19271580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:122359046..122359122hg38UCSC Ensembl
Outerchr5:121694741..121694817hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979072
SamplesKWS2
Known GenesSNCAIP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140364
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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