A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006879



Internal ID19096097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49387474..49464868hg38UCSC Ensembl
Innerchr1:49853146..49930540hg19UCSC Ensembl
Innerchr1:49625733..49703127hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3877395
hg1977395
hg1877395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3700662
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)nsv1006879
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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