A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027480



Internal ID19116699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..316401hg38UCSC Ensembl
Innerchr6:257341..316401hg19UCSC Ensembl
Innerchr6:202341..261401hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3859061
hg1959061
hg1859061
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5882n100
Supporting Variantsnssv3651547, nssv3747615, nssv3747617, nssv3651553, nssv3651544, nssv3651556, nssv3651552, nssv3747618, nssv3651554, nssv3651549, nssv3651548, nssv3651555, nssv3651551, nssv3651557, nssv3747611, nssv3651550, nssv3747614, nssv3747612, nssv3651545, nssv3747613, nssv3747616, nssv3651543, nssv3651546
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)nsv1027480
Frequency
Sample Size11257
Observed Gain13
Observed Loss10
Observed Complex0
Frequencyn/a


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