A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521



Internal ID15204753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:44815733..44848416hg38UCSC Ensembl
Outerchr10:45311181..45343864hg19UCSC Ensembl
Outerchr10:44631187..44663870hg18UCSC Ensembl
Outerchr10:44631187..44663870hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386596
hg196596
hg186596
hg176596
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5288
SamplesNA19129
Known GenesTMEM72-AS1
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)nsv6521
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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