A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110984



Internal ID19256314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98328029..98343577hg38UCSC Ensembl
Outerchr9:101090311..101105859hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3815549
hg1915549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961413
SamplesKWS1
Known GenesGABBR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110984
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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