A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019096



Internal ID19108314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:351292..375265hg38UCSC Ensembl
Innerchr6:351292..375265hg19UCSC Ensembl
Innerchr6:296292..320265hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3823974
hg1923974
hg1823974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5907n100
Supporting Variantsnssv3654672
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)nsv1019096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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