A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3479266



Internal ID19068557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49788283..49934358hg38UCSC Ensembl
Innerchr1:50253955..50400030hg19UCSC Ensembl
Innerchr1:50026542..50172617hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38146076
hg19146076
hg18146076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998640
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)nssv3479266
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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