A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1466n106



Internal ID22795294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43227257..43323854hg38UCSC Ensembl
chr17:41379304..41401222hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3896598
hg1921919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1116524, nsv1129312
SamplesKWS2, KWS1
Known GenesLINC00854
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1466n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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