A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3015n223



Internal ID22805983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16739101..16856000hg38UCSC Ensembl
chr17:16642415..16759314hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38116900
hg19116900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6510963, nsv6497519, nsv6503157
Samples
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3015n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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