A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10771



Internal ID15542027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:87227959..87373779hg38UCSC Ensembl
Outerchr10:88987716..89133536hg19UCSC Ensembl
Outerchr10:88977696..89123516hg18UCSC Ensembl
Outerchr10:88977696..89123516hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38145821
hg19145821
hg18145821
hg17145821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7483
Supporting Variants
SamplesNA18956
Known GenesLOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
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)nssv10771
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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