A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544942



Internal ID15985665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1028586..1035844hg38UCSC Ensembl
Innerchr1:963966..971224hg19UCSC Ensembl
Innerchr1:953829..961087hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg387259
hg197259
hg187259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18n54
Supporting Variantsnssv708484, nssv708485, nssv708490, nssv708486, nssv708491, nssv708489, nssv708487, nssv708488, nssv708483
Samples
Known GenesAGRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544942
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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