A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009478



Internal ID19098696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:195861190..195907849hg38UCSC Ensembl
Innerchr1:195830320..195876979hg19UCSC Ensembl
Innerchr1:194096943..194143602hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3846660
hg1946660
hg1846660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv502n100
Supporting Variantsnssv3704886
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009478
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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