A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155369



Internal ID22085874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3583886..3862438hg38UCSC Ensembl
Outerchr17:3581074..3872622hg38UCSC Ensembl
Innerchr17:3487180..3765732hg19UCSC Ensembl
Outerchr17:3484368..3775916hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38291549
hg19291549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010077
Samples
Known GenesC17orf85, CAMKK1, CTNS, EMC6, GSG2, ITGAE, P2RX5, P2RX5-TAX1BP3, SHPK, TAX1BP3, TRPV1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155369
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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