A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116486



Internal ID18930263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25287254..25287800hg38UCSC Ensembl
Outerchr1:25613745..25614291hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983493, nssv3962777
SamplesKWS1, KWS2
Known GenesRHD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116486
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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