A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125431



Internal ID19262072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:40031055..40057108hg38UCSC Ensembl
Outerchr8:39888574..39914627hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3826054
hg1926054
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983604
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125431
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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