A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584510



Internal ID18536105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64143573..64324788hg38UCSC Ensembl
Innerchr20:62774926..62956141hg19UCSC Ensembl
Innerchr20:62245370..62426585hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38181216
hg19181216
hg18181216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067195
Supporting Variants
Samples
Known GenesLINC00266-1, MYT1, PCMTD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584510
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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