A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7012n100



Internal ID20158628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10747928..10805045hg38UCSC Ensembl
chr8:10605438..10662555hg19UCSC Ensembl
chr8:10642848..10699965hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3857118
hg1957118
hg1857118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031709, nsv1024806
Samples
Known GenesPINX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7012n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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