A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11119



Internal ID15539460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:167129589..167160951hg38UCSC Ensembl
Outerchr1:167098826..167130188hg19UCSC Ensembl
Outerchr1:165365450..165396812hg18UCSC Ensembl
Outerchr1:163830484..163861846hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg388512
hg198512
hg188512
hg178512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3410
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11119
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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