A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952365



Internal ID17301239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:73805562..73812961hg38UCSC Ensembl
Outerchr17:71801701..71809100hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998798
SamplesBILGI_BIOE
Known GenesLINC00469
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952365
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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