A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1586



Internal ID15546149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:69497307..69528995hg38UCSC Ensembl
Outerchr15:69789646..69821334hg19UCSC Ensembl
Outerchr15:67576700..67608388hg18UCSC Ensembl
Outerchr15:67576700..67608388hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387812
hg197812
hg187812
hg177812
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10060
SamplesNA18956
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)nsv1586
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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