A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1674



Internal ID15546237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:92637781..92671702hg38UCSC Ensembl
Outerchr15:93181011..93214932hg19UCSC Ensembl
Outerchr15:90982015..91015936hg18UCSC Ensembl
Outerchr15:90982015..91015936hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385512
hg195512
hg185512
hg175512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7216
SamplesNA12156
Known GenesFAM174B
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)nsv1674
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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