A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133094



Internal ID19268074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:78358363..78359687hg38UCSC Ensembl
Outerchr5:77654187..77655511hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987906
SamplesKWS1
Known GenesLOC728769
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133094
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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