A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954598



Internal ID16956785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:61270039..61270111hg38UCSC Ensembl
Outerchr17:59347400..59347472hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002660
SamplesBILGI_BIOE
Known GenesBCAS3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954598
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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