A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116543



Internal ID19256776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:10004297..10015260hg38UCSC Ensembl
Outerchr5:10004409..10015372hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3810964
hg1910964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978725
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116543
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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