A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025122



Internal ID19114340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..384097hg38UCSC Ensembl
Innerchr6:257341..384097hg19UCSC Ensembl
Innerchr6:202341..329097hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38126757
hg19126757
hg18126757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3652642, nssv3652636, nssv3652637, nssv3652639, nssv3652640, nssv3652638, nssv3652641, nssv3747733
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)nsv1025122
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer