A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023821



Internal ID19113038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:250549..350608hg38UCSC Ensembl
Innerchr6:250549..350608hg19UCSC Ensembl
Innerchr6:195549..295608hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38100060
hg19100060
hg18100060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5877n100
Supporting Variantsnssv3650392
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)nsv1023821
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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