A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2577n106



Internal ID20161934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111556217..111556961hg38UCSC Ensembl
chr3:111275064..111275808hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1129412, nsv1141977
SamplesKWS1, KWS2
Known GenesCD96
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2577n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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