A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120074



Internal ID19286622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:168119201..168119287hg38UCSC Ensembl
Outerchr1:168088439..168088525hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960818
SamplesKWS1
Known GenesGPR161
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120074
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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