A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141886



Internal ID18940553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:20539894..20771229hg38UCSC Ensembl
Outerchr19:20722700..20954035hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38231336
hg19231336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993393
SamplesKWS2
Known GenesZNF626, ZNF737
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141886
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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