A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1675



Internal ID15199552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:92825331..92860622hg38UCSC Ensembl
Outerchr15:93368561..93403852hg19UCSC Ensembl
Outerchr15:91169565..91204856hg18UCSC Ensembl
Outerchr15:91169565..91204856hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384446
hg194446
hg184446
hg174446
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4175
SamplesNA12878
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)nsv1675
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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