A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022504



Internal ID19111722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..385772hg38UCSC Ensembl
Innerchr6:257341..385772hg19UCSC Ensembl
Innerchr6:202341..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38128432
hg19128432
hg18128432
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3652662, nssv3652655, nssv3652668, nssv3652656, nssv3652643, nssv3652664, nssv3652644, nssv3652653, nssv3652661, nssv3652667, nssv3652647, nssv3652659, nssv3652649, nssv3652648, nssv3652646, nssv3652658, nssv3652652, nssv3652651, nssv3652663, nssv3652650, nssv3652665, nssv3652660, nssv3652666, nssv3652645, nssv3652654, nssv3652657
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)nsv1022504
Frequency
Sample Size11257
Observed Gain6
Observed Loss20
Observed Complex0
Frequencyn/a


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