A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548355



Internal ID15989078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180783489..180786185hg38UCSC Ensembl
Innerchr1:180752625..180755321hg19UCSC Ensembl
Innerchr1:179019248..179021944hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg382697
hg192697
hg182697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv729733, nssv729732, nssv729730, nssv729731, nssv729734
Samples
Known GenesXPR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548355
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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