A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1690



Internal ID15194287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:142153176..142215263hg18UCSC Ensembl
Outerchr7:141959891..142021978hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg1862088
hg1762088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5982
Supporting Variants
SamplesNA18555
Known GenesPRSS2, PRSS3P2
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)nssv1690
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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