A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007779



Internal ID22069410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:198979470..198987456hg38UCSC Ensembl
Outerchr1:198977059..198987756hg38UCSC Ensembl
Innerchr1:198948599..198956585hg19UCSC Ensembl
Outerchr1:198946188..198956885hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3810698
hg1910698
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154539
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007779
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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