A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978707



Internal ID18890924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:601650..601714hg38UCSC Ensembl
Outerchr19:601650..601714hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116526
Supporting Variants
SamplesKWS2
Known GenesHCN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978707
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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