A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141859



Internal ID19278919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:118771427..118773043hg38UCSC Ensembl
Outerchr2:119529003..119530619hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg381617
hg191617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2009n106
Supporting Variantsnssv3993365
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141859
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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