A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8815



Internal ID15188363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76489376..76510062hg38UCSC Ensembl
Outerchr10:78249134..78269820hg19UCSC Ensembl
Outerchr10:77919140..77939826hg18UCSC Ensembl
Outerchr10:77919140..77939826hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3820687
hg1920687
hg1820687
hg1720687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7243
Supporting Variants
SamplesNA12156
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)nssv8815
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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