A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058264



Internal ID19147483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32042851..32082495hg38UCSC Ensembl
Innerchr21:33415164..33454808hg19UCSC Ensembl
Innerchr21:32337035..32376679hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3839645
hg1939645
hg1839645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600123
Samples
Known GenesLINC00159
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058264
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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