A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719025



Internal ID15666295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89011781..89013290hg38UCSC Ensembl
Innerchr1:89477464..89478973hg19UCSC Ensembl
Innerchr1:89250052..89251561hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381510
hg191510
hg181510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546793
Supporting Variants
Samples
Known GenesGBP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719025
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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