A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125287



Internal ID19258913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:170170742..170171983hg38UCSC Ensembl
Outerchr5:169597746..169598987hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3211n106
Supporting Variantsnssv3983458
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125287
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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