A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983611



Internal ID19229875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:14877435..14880332hg38UCSC Ensembl
Outerchr9:14877433..14880330hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382898
hg192898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125437
Supporting Variants
SamplesKWS2
Known GenesFREM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983611
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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