A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6665



Internal ID15204911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:51440247..51461733hg38UCSC Ensembl
Outerchr10:53200007..53221493hg19UCSC Ensembl
Outerchr10:52870013..52891499hg18UCSC Ensembl
Outerchr10:52870013..52891499hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3821487
hg1921487
hg1821487
hg1721487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3879
SamplesNA12878
Known GenesPRKG1
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)nsv6665
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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