A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147329



Internal ID19196366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:48853575..48919272hg38UCSC Ensembl
Outerchr7:48893171..48958868hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3865698
hg1965698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000106
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147329
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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