A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055623



Internal ID19144842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38746527..38789148hg38UCSC Ensembl
Innerchr21:40118451..40161072hg19UCSC Ensembl
Innerchr21:39040321..39082942hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3842622
hg1942622
hg1842622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4432n100
Supporting Variantsnssv3600204
Samples
Known GenesLINC00114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055623
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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