A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978662



Internal ID18894167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114302719..114303290hg38UCSC Ensembl
Outerchr9:117064999..117065570hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116481
Supporting Variants
SamplesKWS2
Known GenesCOL27A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978662
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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