A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022899



Internal ID19112116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..382559hg38UCSC Ensembl
Innerchr6:264744..382559hg19UCSC Ensembl
Innerchr6:209744..327559hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38117816
hg19117816
hg18117816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3747793, nssv3653597
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)nsv1022899
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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