A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155473



Internal ID22085978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46554684..46674934hg38UCSC Ensembl
Outerchr17:46494937..46687628hg38UCSC Ensembl
Innerchr17:44632050..44752300hg19UCSC Ensembl
Outerchr17:44572303..44764994hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38192692
hg19192692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n97
Supporting Variantsnssv4011837, nssv4011838, nssv4011840, nssv4011839, nssv4011841, nssv4011835, nssv4011836
Samples
Known GenesARL17A, LRRC37A2, NSF, NSFP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155473
Frequency
Sample Size131
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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