A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv410



Internal ID15202089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:3635087..3667080hg38UCSC Ensembl
Outerchr1:3551651..3583644hg19UCSC Ensembl
Outerchr1:3541511..3573504hg18UCSC Ensembl
Outerchr1:3574808..3606801hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg387510
hg197510
hg187510
hg177510
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10069
SamplesNA18956
Known GenesTP73, WRAP73
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)nsv410
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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