A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133027



Internal ID19253254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:91040251..91040331hg38UCSC Ensembl
Outerchr1:91505808..91505888hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987824
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133027
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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