A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3097n100



Internal ID20154713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9026594..9059170hg38UCSC Ensembl
chr17:8929911..8962487hg19UCSC Ensembl
chr17:8870636..8903212hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3832577
hg1932577
hg1832577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056444, nsv1063537
Samples
Known GenesNTN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3097n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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