A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000872



Internal ID19090089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40564081..40601959hg38UCSC Ensembl
Innerchr2:40791221..40829099hg19UCSC Ensembl
Innerchr2:40644725..40682603hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3837879
hg1937879
hg1837879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581487
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000872
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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