A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501005



Internal ID20874235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35882977..36193981hg38UCSC Ensembl
chr17:34209981..34521380hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38311005
hg19311400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n223
Supporting Variantsnssv18182340
Samples
Known GenesCCL14, CCL15, CCL15-CCL14, CCL16, CCL18, CCL23, CCL3, CCL4, LYZL6, RDM1, TBC1D3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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