A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7243



Internal ID15205547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76482957..76510163hg38UCSC Ensembl
Outerchr10:78242715..78269921hg19UCSC Ensembl
Outerchr10:77912721..77939927hg18UCSC Ensembl
Outerchr10:77912721..77939927hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3827207
hg1927207
hg1827207
hg1727207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8815, nssv1901, nssv3884
SamplesNA12156, NA12878, NA18555
Known GenesC10orf11
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)nsv7243
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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