A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7572



Internal ID15552595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:120447233..120474549hg38UCSC Ensembl
Outerchr10:122206745..122234061hg19UCSC Ensembl
Outerchr10:122196735..122224051hg18UCSC Ensembl
Outerchr10:122196735..122224051hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3827317
hg1927317
hg1827317
hg1727317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8852
SamplesNA12156
Known GenesPPAPDC1A
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)nsv7572
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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