A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1701n106



Internal ID20161058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7035377..7054271hg38UCSC Ensembl
chr19:7035388..7054282hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3818895
hg1918895
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1129313, nsv1129318
SamplesKWS1
Known GenesMBD3L2, MBD3L4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1701n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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