A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9537



Internal ID15539777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:5882443..5897524hg38UCSC Ensembl
Outerchr17:5785763..5800844hg19UCSC Ensembl
Outerchr17:5726487..5741568hg18UCSC Ensembl
Outerchr17:5726487..5741568hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3821612
hg1921612
hg1821612
hg1721612
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1958
Supporting Variants
SamplesNA18507
Known GenesLOC339166
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)nssv9537
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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