A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058614



Internal ID19147833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22064367..22168160hg38UCSC Ensembl
Innerchr20:22045005..22148798hg19UCSC Ensembl
Innerchr20:21993005..22096798hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38103794
hg19103794
hg18103794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4285n100
Supporting Variantsnssv3737175, nssv3584656
Samples
Known GenesLOC100270679
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058614
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer