A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3480937



Internal ID19069448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49449248..49536563hg38UCSC Ensembl
Innerchr1:49914920..50002235hg19UCSC Ensembl
Innerchr1:49687507..49774822hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3887316
hg1987316
hg1887316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001600
Supporting Variants
Samples
Known GenesAGBL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3480937
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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