A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997300



Internal ID19156838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:360262..453210hg38UCSC Ensembl
Innerchr4:354051..446999hg19UCSC Ensembl
Innerchr4:344051..436999hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3892949
hg1992949
hg1892949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5077n100
Supporting Variantsnssv3616092
Samples
Known GenesABCA11P, ZNF141, ZNF721
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997300
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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