A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010476



Internal ID19099693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49558898..49954717hg38UCSC Ensembl
Innerchr1:50024570..50420389hg19UCSC Ensembl
Innerchr1:49797157..50192976hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38395820
hg19395820
hg18395820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv164n100
Supporting Variantsnssv3470174
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)nsv1010476
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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