A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031714



Internal ID19120936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:258253..381137hg38UCSC Ensembl
Innerchr6:258253..381137hg19UCSC Ensembl
Innerchr6:203253..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38122885
hg19122885
hg18122885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3652722, nssv3747750, nssv3652723, nssv3652721, nssv3652719, nssv3747746, nssv3747747, nssv3747751, nssv3747748, nssv3652720, nssv3747749
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)nsv1031714
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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