A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625665



Internal ID15502512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:43181451..43181920hg38UCSC Ensembl
Outerchr10:43676899..43677368hg19UCSC Ensembl
Outerchr10:42996905..42997374hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381313
hg191313
hg181313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513008
Supporting Variants
Samples1
Known GenesCSGALNACT2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625665
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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