A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129434



Internal ID19280726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:13862117..13890319hg38UCSC Ensembl
Outerchr7:13901742..13929944hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3828203
hg1928203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962880
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129434
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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