A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140267



Internal ID19275643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:175231433..175232798hg38UCSC Ensembl
Outerchr1:175200569..175201934hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978979
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140267
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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