A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987875



Internal ID19210875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29819009..29819076hg38UCSC Ensembl
Outerchr19:30309916..30309983hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133066
Supporting Variants
SamplesKWS1
Known GenesCCNE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987875
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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