A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120070



Internal ID19258670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:27201943..27202172hg38UCSC Ensembl
Outerchr1:27528434..27528663hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960812
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120070
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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