A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6282n100



Internal ID22792369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13616511..13693981hg38UCSC Ensembl
chr7:13656136..13733606hg19UCSC Ensembl
chr7:13622661..13700131hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3877471
hg1977471
hg1877471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017322, nsv1017756
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6282n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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