A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962753



Internal ID19213925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:172455537..172456233hg38UCSC Ensembl
Outerchr3:172173327..172174023hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129320
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962753
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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