A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004296



Internal ID19093513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:17040041..17065867hg38UCSC Ensembl
Innerchr2:17221308..17247134hg19UCSC Ensembl
Innerchr2:17084789..17110615hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3825827
hg1925827
hg1825827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3732n100
Supporting Variantsnssv3578912
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)nsv1004296
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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