A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1099



Internal ID15198976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:61809645..61850271hg38UCSC Ensembl
Outerchr1:62275317..62315943hg19UCSC Ensembl
Outerchr1:62047905..62088531hg18UCSC Ensembl
Outerchr1:61987338..62027964hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3840627
hg1940627
hg1840627
hg1740627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9211
SamplesNA12156
Known GenesINADL
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)nsv1099
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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