A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1508



Internal ID15199385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:42464653..42498668hg38UCSC Ensembl
Outerchr15:42756851..42790866hg19UCSC Ensembl
Outerchr15:40544143..40578158hg18UCSC Ensembl
Outerchr15:40544143..40578158hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg385688
hg195688
hg185688
hg175688
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4149
SamplesNA12878
Known GenesSNAP23, ZNF106
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)nsv1508
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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