A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021606



Internal ID19110824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:258253..315197hg38UCSC Ensembl
Innerchr6:258253..315197hg19UCSC Ensembl
Innerchr6:203253..260197hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3856945
hg1956945
hg1856945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5885n100
Supporting Variantsnssv3652706
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)nsv1021606
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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