A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3276n100



Internal ID22789363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67112406..67203537hg38UCSC Ensembl
chr17:65108522..65199653hg19UCSC Ensembl
chr17:62538984..62630115hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3891132
hg1991132
hg1891132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064151, nsv1059646, nsv1057500
Samples
Known GenesHELZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3276n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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