A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3285n100



Internal ID20154901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78595683..78678139hg38UCSC Ensembl
chr17:76591765..76674221hg19UCSC Ensembl
chr17:74103360..74185816hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3882457
hg1982457
hg1882457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067328, nsv1056689, nsv1066466
Samples
Known GenesCYTH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3285n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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