A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801



Internal ID15197964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28200147..28225139hg38UCSC Ensembl
Outerchr10:28489076..28514068hg19UCSC Ensembl
Outerchr10:28529082..28554074hg18UCSC Ensembl
Outerchr10:28529082..28554074hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3824993
hg1924993
hg1824993
hg1724993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6188
Supporting Variants
SamplesNA19240
Known GenesMPP7
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)nssv801
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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