A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6259n100



Internal ID22792346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8844447..9152943hg38UCSC Ensembl
chr7:8884077..9192573hg19UCSC Ensembl
chr7:8850602..9159098hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38308497
hg19308497
hg18308497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020577, nsv1019893
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)dgv6259n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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