A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7588



Internal ID15552612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124377686..124396525hg38UCSC Ensembl
Outerchr10:126066255..126085094hg19UCSC Ensembl
Outerchr10:126056245..126075084hg18UCSC Ensembl
Outerchr10:126056245..126075084hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3818840
hg1918840
hg1818840
hg1718840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv969
SamplesNA19240
Known Genes
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)nsv7588
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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