A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1361



Internal ID15544354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:27330332..27365632hg38UCSC Ensembl
Outerchr17:25657358..25692658hg19UCSC Ensembl
Outerchr17:22681485..22716785hg18UCSC Ensembl
Outerchr17:22681485..22716785hg17UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg385683
hg195683
hg185683
hg175683
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2013
Supporting Variants
SamplesNA19240
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)nssv1361
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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