A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545913



Internal ID16333322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27522789..27610945hg38UCSC Ensembl
Innerchr1:27849300..27937456hg19UCSC Ensembl
Innerchr1:27721887..27810043hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3888157
hg1988157
hg1888157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv220n54
Supporting Variantsnssv1173804
SamplesHGDP00890
Known GenesAHDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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