A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033255



Internal ID19122477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..320860hg38UCSC Ensembl
Innerchr6:257341..320860hg19UCSC Ensembl
Innerchr6:202341..265860hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3863520
hg1963520
hg1863520
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5882n100
Supporting Variantsnssv3651563, nssv3651562, nssv3651564, nssv3651561, nssv3651559, nssv3747620, nssv3747619, nssv3651560, nssv3747621
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)nsv1033255
Frequency
Sample Size11257
Observed Gain4
Observed Loss5
Observed Complex0
Frequencyn/a


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