A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061325



Internal ID19150544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62448564..62561745hg38UCSC Ensembl
Innerchr20:61023620..61158952hg19UCSC Ensembl
Innerchr20:60457015..60569397hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38113182
hg19135333
hg18112383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4344n100
Supporting Variantsnssv3584494, nssv3584491, nssv3584485, nssv3584490, nssv3584488, nssv3584486, nssv3584492, nssv3584487, nssv3584484, nssv3584493, nssv3584489
Samples
Known GenesC20orf166, C20orf166-AS1, GATA5, MIR1-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061325
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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