A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013568



Internal ID19102787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18985650..19053148hg38UCSC Ensembl
Innerchr2:19166928..19252904hg19UCSC Ensembl
Innerchr2:19030409..19116385hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3867499
hg1985977
hg1885977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3578981
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)nsv1013568
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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