A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960938



Internal ID19217577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107714476..107721289hg38UCSC Ensembl
Outerchr9:110476757..110483570hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg386814
hg196814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120177
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960938
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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