A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110855



Internal ID18906299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:52221895..52584579hg38UCSC Ensembl
Outerchr13:52796030..53158714hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38362685
hg19362685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961265
SamplesKWS1
Known GenesCKAP2, THSD1, TPTE2P3, VPS36
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110855
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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