A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019810



Internal ID19109028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..364474hg38UCSC Ensembl
Innerchr6:257341..364474hg19UCSC Ensembl
Innerchr6:202341..309474hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38107134
hg19107134
hg18107134
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3651652, nssv3651651, nssv3651653
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)nsv1019810
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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