A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7508



Internal ID15552524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97525618..97570744hg38UCSC Ensembl
Outerchr10:99285375..99330501hg19UCSC Ensembl
Outerchr10:99275365..99320491hg18UCSC Ensembl
Outerchr10:99275365..99320491hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3845127
hg1945127
hg1845127
hg1745127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5307
SamplesNA19129
Known GenesUBTD1
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)nsv7508
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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