A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3700852



Internal ID18999133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:20229536..20277521hg38UCSC Ensembl
Innerchr1:20556029..20604014hg19UCSC Ensembl
Innerchr1:20428616..20476601hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3847986
hg1947986
hg1847986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000821
Supporting Variants
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)nssv3700852
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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