A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv733898



Internal ID16027854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:194802203..194863360hg38UCSC Ensembl
Innerchr1:194771333..194832490hg19UCSC Ensembl
Innerchr1:193037956..193099113hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3861158
hg1961158
hg1861158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548697
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv733898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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