A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5642



Internal ID15543793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:17047941..17065227hg38UCSC Ensembl
Outerchr17:16951255..16968541hg19UCSC Ensembl
Outerchr17:16891980..16909266hg18UCSC Ensembl
Outerchr17:16891980..16909266hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3814077
hg1914077
hg1814077
hg1714077
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1995
Supporting Variants
SamplesNA19129
Known GenesMPRIP
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)nssv5642
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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