A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997267



Internal ID19156805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:45522504..45701109hg38UCSC Ensembl
Innerchr4:45524521..45703126hg19UCSC Ensembl
Innerchr4:45219278..45397883hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38178606
hg19178606
hg18178606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739401
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)nsv997267
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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