A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003752



Internal ID19092970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3847117..3875579hg38UCSC Ensembl
Innerchr2:3894707..3923169hg19UCSC Ensembl
Innerchr2:3872582..3901044hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3828463
hg1928463
hg1828463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3703n100
Supporting Variantsnssv3571304
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)nsv1003752
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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