A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv127n97



Internal ID22815524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16729340..16836956hg38UCSC Ensembl
chr17:16632654..16740270hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38107617
hg19107617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155385, nsv1155382, nsv1155384, nsv1155386
Samples
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv127n97
Frequency
Sample Size131
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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