A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993452



Internal ID18882563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:4899348..4899416hg38UCSC Ensembl
Outerchr19:4899360..4899428hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141946
Supporting Variants
SamplesKWS2
Known GenesARRDC5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993452
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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