A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003151



Internal ID19092368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49382052..49496947hg38UCSC Ensembl
Innerchr1:49847724..49962619hg19UCSC Ensembl
Innerchr1:49620311..49735206hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38114896
hg19114896
hg18114896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3700661
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)nsv1003151
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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