A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058372



Internal ID19147591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22064367..22173462hg38UCSC Ensembl
Innerchr20:22045005..22154100hg19UCSC Ensembl
Innerchr20:21993005..22102100hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38109096
hg19109096
hg18109096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4285n100
Supporting Variantsnssv3584657, nssv3737176
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)nsv1058372
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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