A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067365



Internal ID19156584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45719911..45754523hg38UCSC Ensembl
Innerchr20:44348550..44383162hg19UCSC Ensembl
Innerchr20:43781964..43816569hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3834613
hg1934613
hg1834606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n100
Supporting Variantsnssv3584895, nssv3584893, nssv3731339, nssv3731338, nssv3584894
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)nsv1067365
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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