A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061414



Internal ID18803945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45721722..45746167hg38UCSC Ensembl
Innerchr20:44350361..44374806hg19UCSC Ensembl
Innerchr20:43783775..43808213hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3824446
hg1924446
hg1824439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n100
Supporting Variantsnssv3584896
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061414
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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