A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110885



Internal ID18933299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:4973914..4994163hg38UCSC Ensembl
Outerchr10:5016106..5036355hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3820250
hg1920250
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv349n106
Supporting Variantsnssv3961297
SamplesKWS1
Known GenesAKR1C1, AKR1C2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110885
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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