A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003855



Internal ID19093073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9904926..9919715hg38UCSC Ensembl
Innerchr2:10045055..10059844hg19UCSC Ensembl
Innerchr2:9962506..9977295hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3814790
hg1914790
hg1814790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576957
Samples
Known GenesTAF1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003855
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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