A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6298n100



Internal ID22792385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17662511..17694130hg38UCSC Ensembl
chr7:17702135..17733754hg19UCSC Ensembl
chr7:17668660..17700279hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3831620
hg1931620
hg1831620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023105, nsv1031163
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)dgv6298n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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