A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv956



Internal ID15198492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:87232304..87405077hg38UCSC Ensembl
Outerchr10:88992061..89164834hg19UCSC Ensembl
Outerchr10:88982041..89154814hg18UCSC Ensembl
Outerchr10:88982041..89154814hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38172774
hg19172774
hg18172774
hg17172774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7483
Supporting Variants
SamplesNA19240
Known GenesLINC00864, LOC439994, 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)nssv956
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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