A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7174n100



Internal ID22793261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39378072..39531593hg38UCSC Ensembl
chr8:39235591..39389112hg19UCSC Ensembl
chr8:39354748..39508269hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38153522
hg19153522
hg18153522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028060, nsv1032940, nsv1033648, nsv1015409
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)dgv7174n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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