A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2209



Internal ID15546772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:13276411..13316571hg38UCSC Ensembl
Outerchr18:13276410..13316570hg19UCSC Ensembl
Outerchr18:13266410..13306570hg18UCSC Ensembl
Outerchr18:13266410..13306570hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3840161
hg1940161
hg1840161
hg1740161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7367
SamplesNA12156
Known GenesLDLRAD4
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)nsv2209
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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