A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7169n100



Internal ID22793256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39372652..39485418hg38UCSC Ensembl
chr8:39230171..39342937hg19UCSC Ensembl
chr8:39349328..39462094hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38112767
hg19112767
hg18112767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018341, nsv1032337, nsv1018880
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7169n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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