A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv729765



Internal ID15677035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:182808616..182817818hg38UCSC Ensembl
Innerchr1:182777751..182786953hg19UCSC Ensembl
Innerchr1:181044374..181053576hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg389203
hg199203
hg189203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548370
Supporting Variants
Samples
Known GenesNPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv729765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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