A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv475962



Internal ID15575396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227598488..227598488hg38UCSC Ensembl
chr1:227786189..227786189hg19UCSC Ensembl
chr1:225852812..225852812hg18UCSC Ensembl
chr1:224092924..224092924hg17UCSC Ensembl
Cytoband1q42.13
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 Variantsnssv3019705
SamplesNA12878
Known GenesZNF678
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)nsv475962
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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