A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148187



Internal ID19197014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:14808045..14875677hg38UCSC Ensembl
Outerchr5:14808154..14875786hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3867633
hg1967633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001698
SamplesKWB1
Known GenesANKH, MIR4637
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148187
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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