A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712053



Internal ID15659323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28648638..28678234hg38UCSC Ensembl
Innerchr1:28975150..29004746hg19UCSC Ensembl
Innerchr1:28847737..28877333hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3829597
hg1929597
hg1829597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545920
Supporting Variants
Samples
Known GenesGMEB1, RNU11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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