A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3298



Internal ID15547893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:14585811..14612990hg38UCSC Ensembl
Outerchr1:14912307..14939486hg19UCSC Ensembl
Outerchr1:14784894..14812073hg18UCSC Ensembl
Outerchr1:14657613..14684792hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg386660
hg196660
hg186660
hg176660
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7914
SamplesNA12156
Known GenesKAZN
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)nsv3298
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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