A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3159n100



Internal ID22789246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41231296..41274267hg38UCSC Ensembl
chr17:39387548..39430519hg19UCSC Ensembl
chr17:36641074..36684045hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3842972
hg1942972
hg1842972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061320, nsv1058815, nsv1060445
Samples
Known GenesKRTAP9-3, KRTAP9-4, KRTAP9-6, KRTAP9-8, KRTAP9-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3159n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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