A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979028



Internal ID19226254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:77225751..77248111hg38UCSC Ensembl
Outerchr18:74937707..74960067hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3822361
hg1922361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140317
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979028
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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