A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9914



Internal ID15539997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:158310855..158348125hg38UCSC Ensembl
Outerchr7:158103547..158140817hg19UCSC Ensembl
Outerchr7:157796308..157833578hg18UCSC Ensembl
Outerchr7:157603023..157640293hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3837271
hg1937271
hg1837271
hg1737271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6027
Supporting Variants
SamplesNA18507
Known GenesPTPRN2
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)nssv9914
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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