A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979026



Internal ID19229936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26881388..26881482hg38UCSC Ensembl
Outerchr18:24461352..24461446hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140315
Supporting Variants
SamplesKWS2
Known GenesAQP4-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979026
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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