A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10783



Internal ID15195329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122992789..123005766hg38UCSC Ensembl
Outerchr10:124752305..124765282hg19UCSC Ensembl
Outerchr10:124742295..124755272hg18UCSC Ensembl
Outerchr10:124742295..124755272hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386736
hg196736
hg186736
hg176736
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7586
Supporting Variants
SamplesNA18956
Known GenesIKZF5
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)nssv10783
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer