A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3269n100



Internal ID22789356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57210510..57230319hg38UCSC Ensembl
chr17:55287871..55307680hg19UCSC Ensembl
chr17:52642870..52662679hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3819810
hg1919810
hg1819810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061415, nsv1055884
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)dgv3269n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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