A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011869



Internal ID22073500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59290376..59444934hg38UCSC Ensembl
Outerchr17:59269345..59449552hg38UCSC Ensembl
Innerchr17:57367737..57522295hg19UCSC Ensembl
Outerchr17:57346706..57526913hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38180208
hg19180208
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155489
Supporting Variants
Samples
Known GenesGDPD1, MIR4729, YPEL2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011869
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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