A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1195e199



Internal ID22758968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39506546..39514643hg38UCSC Ensembl
chr7:39546145..39554242hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg388098
hg198098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672925, esv2666474
SamplesHG01462, HG00187, HG00318, HG00177, HG01140, HG01488, HG00282, HG00328, HG01149, HG01497, HG00285, HG01375, HG01137, HG01489, HG00342, HG00174, HG00280, HG00343, HG00372, HG01125
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1195e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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