A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv474979



Internal ID15227732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166924744..166924744hg38UCSC Ensembl
chr2:167781254..167781254hg19UCSC Ensembl
chr2:167489500..167489500hg18UCSC Ensembl
chr2:167606761..167606761hg17UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3012990
SamplesNA18956
Known GenesXIRP2
MethodSequencing
AnalysisSearch fosmid ESPs as described in Tuzun et al (2005)
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA singleton. The coordinate provided is from the mappable member of a fosmid end sequence pair, and indicates the genomic vicinity of a novel sequence insertion
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nsv474979
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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