A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047471



Internal ID18790002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31321504..31384922hg38UCSC Ensembl
Innerchr10:31610433..31673851hg19UCSC Ensembl
Innerchr10:31650439..31713857hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3863419
hg1963419
hg1863419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv701n100
Supporting Variantsnssv3518643
Samples
Known GenesZEB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047471
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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