A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155384



Internal ID22085889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16754017..16819487hg38UCSC Ensembl
Outerchr17:16750987..16832218hg38UCSC Ensembl
Innerchr17:16657331..16722801hg19UCSC Ensembl
Outerchr17:16654301..16735532hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3881232
hg1981232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127n97
Supporting Variantsnssv4010114, nssv4010116, nssv4010115, nssv4010117
Samples
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155384
Frequency
Sample Size131
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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