A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011949



Internal ID19101167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49299766..49431310hg38UCSC Ensembl
Innerchr1:49765438..49896982hg19UCSC Ensembl
Innerchr1:49538025..49669569hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38131545
hg19131545
hg18131545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3471966
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)nsv1011949
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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