A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993450



Internal ID18900632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:4354680..4354740hg38UCSC Ensembl
Outerchr18:4354680..4354740hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141944
Supporting Variants
SamplesKWS2
Known GenesDLGAP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993450
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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