A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110865



Internal ID18906509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:195644796..195944378hg38UCSC Ensembl
Outerchr3:195371667..195671249hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38299583
hg19299583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2683n106
Supporting Variantsnssv3961276
SamplesKWS1
Known GenesMIR570, MIR6829, MUC20, MUC4, SDHAP2, TNK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110865
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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