A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018768



Internal ID19107985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:258253..303121hg38UCSC Ensembl
Innerchr6:258253..303121hg19UCSC Ensembl
Innerchr6:203253..248121hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3844869
hg1944869
hg1844869
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5881n100
Supporting Variantsnssv3652704, nssv3652702, nssv3652700, nssv3747743, nssv3747744, nssv3652703, nssv3747742, nssv3652705, nssv3652701
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)nsv1018768
Frequency
Sample Size11257
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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