A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120147



Internal ID19280545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:5314721..5314808hg38UCSC Ensembl
Outerchr5:5314834..5314921hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960904
SamplesKWS1
Known GenesADAMTS16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120147
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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