A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv349n106



Internal ID19018458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4973904..4994173hg38UCSC Ensembl
chr10:5016096..5036365hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3820270
hg1920270
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1140270, nsv1110885
SamplesKWS1, KWS2
Known GenesAKR1C1, AKR1C2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv349n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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