A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1550



Internal ID15546113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:58178561..58187617hg38UCSC Ensembl
Outerchr15:58470760..58479816hg19UCSC Ensembl
Outerchr15:56258052..56267108hg18UCSC Ensembl
Outerchr15:56258052..56267108hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385912
hg195912
hg185912
hg175912
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4154
SamplesNA12878
Known GenesAQP9
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)nsv1550
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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