A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032203



Internal ID19121425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:254255..381137hg38UCSC Ensembl
Innerchr6:254255..381137hg19UCSC Ensembl
Innerchr6:199255..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38126883
hg19126883
hg18126883
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3746774, nssv3650448, nssv3650450, nssv3650449
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032203
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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