A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2637n106



Internal ID22796465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172455534..172456273hg38UCSC Ensembl
chr3:172173324..172174063hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1129320, nsv1110838
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2637n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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