A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018436



Internal ID19107653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:271761..381137hg38UCSC Ensembl
Innerchr6:271761..381137hg19UCSC Ensembl
Innerchr6:216761..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38109377
hg19109377
hg18109377
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3653659, nssv3747802, nssv3747801
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)nsv1018436
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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