A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133059



Internal ID19270118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:57013552..57021664hg38UCSC Ensembl
Outerchr17:55090913..55099025hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg388113
hg198113
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987868
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133059
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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