A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010110



Internal ID22071741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15773687..15791471hg38UCSC Ensembl
Outerchr17:15770691..15791687hg38UCSC Ensembl
Innerchr17:15677001..15694785hg19UCSC Ensembl
Outerchr17:15674005..15695001hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3820997
hg1920997
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155380
Supporting Variants
Samples
Known GenesMEIS3P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010110
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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