A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7337n100



Internal ID22793424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144910942..144941493hg38UCSC Ensembl
chr8:146136327..146166879hg19UCSC Ensembl
chr8:146107131..146137683hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3830552
hg1930553
hg1830553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027356, nsv1027878, nsv1027172
Samples
Known GenesZNF16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7337n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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