A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv733983



Internal ID16027939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196774797..196852792hg38UCSC Ensembl
Innerchr1:196743927..196821922hg19UCSC Ensembl
Innerchr1:195010550..195088545hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3877996
hg1977996
hg1877996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548782
Supporting Variants
Samples
Known GenesCFHR1, CFHR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv733983
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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