A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7188



Internal ID15536676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:65973639..65981757hg38UCSC Ensembl
Outerchr15:66265977..66274095hg19UCSC Ensembl
Outerchr15:64053031..64061149hg18UCSC Ensembl
Outerchr15:64053031..64061149hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg386573
hg196573
hg186573
hg176573
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1571
Supporting Variants
SamplesNA12156
Known GenesMEGF11
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)nssv7188
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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