A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv74e199



Internal ID22757847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161514314..161604439hg38UCSC Ensembl
chr1:161484104..161574229hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3890126
hg1990126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658398, esv2661315
SamplesHG00121, HG00351, HG00109, HG01351, HG00359, HG01259, NA19753, HG00381
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv74e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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