A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2015



Internal ID15546578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:27886896..27931711hg38UCSC Ensembl
Outerchr17:26213922..26258737hg19UCSC Ensembl
Outerchr17:23238049..23282864hg18UCSC Ensembl
Outerchr17:23238049..23282864hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3844816
hg1944816
hg1844816
hg1744816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7317
SamplesNA12156
Known GenesLYRM9
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv2015
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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