A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6637



Internal ID15537226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66139882..66172177hg38UCSC Ensembl
Outerchr15:66432220..66464515hg19UCSC Ensembl
Outerchr15:64219274..64251569hg18UCSC Ensembl
Outerchr15:64219274..64251569hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg387144
hg197144
hg187144
hg177144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1574
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)nssv6637
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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