A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125411



Internal ID18938732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:56804955..56833027hg38UCSC Ensembl
Outerchr5:56100782..56128854hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3828073
hg1928073
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983582
SamplesKWS2
Known GenesMAP3K1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125411
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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