A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141942



Internal ID18932958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:73137299..73137857hg38UCSC Ensembl
Outerchr17:71133438..71133996hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993447
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141942
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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