A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589965



Internal ID18888246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:886300..955436hg38UCSC Ensembl
Innerchr20:866943..936079hg19UCSC Ensembl
Innerchr20:814943..884079hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3869137
hg1969137
hg1869137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062764
Supporting Variants
Samples
Known GenesANGPT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589965
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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