A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498266



Internal ID20871475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33631491..34610756hg38UCSC Ensembl
chr17:31958510..32937775hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38979266
hg19979266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183364
Samples
Known GenesASIC2, C17orf102, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8, TMEM132E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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