A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv733998



Internal ID16027954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196780615..196852792hg38UCSC Ensembl
Innerchr1:196749745..196821922hg19UCSC Ensembl
Innerchr1:195016368..195088545hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3872178
hg1972178
hg1872178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548793
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)nssv733998
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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