A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10778



Internal ID15542020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:109802929..109825914hg38UCSC Ensembl
Outerchr10:111562687..111585672hg19UCSC Ensembl
Outerchr10:111552677..111575662hg18UCSC Ensembl
Outerchr10:111552677..111575662hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3822986
hg1922986
hg1822986
hg1722986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7545
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10778
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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