A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141944



Internal ID18909788
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 StatusM
Merged Variants
Supporting Variantsnssv3993450
SamplesKWS2
Known GenesDLGAP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141944
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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