A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961343



Internal ID18866587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:16402722..16402779hg38UCSC Ensembl
Outerchr19:16513533..16513590hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110925
Supporting Variants
SamplesKWS1
Known GenesEPS15L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961343
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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