A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027634



Internal ID19116853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:331800..381137hg38UCSC Ensembl
Innerchr6:331800..381137hg19UCSC Ensembl
Innerchr6:276800..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3849338
hg1949338
hg1849338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5899n100
Supporting Variantsnssv3654635, nssv3654634, nssv3654633
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)nsv1027634
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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