A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021334



Internal ID19110551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:314950..364970hg38UCSC Ensembl
Innerchr6:314950..364970hg19UCSC Ensembl
Innerchr6:259950..309970hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3850021
hg1950021
hg1850021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5894n100
Supporting Variantsnssv3653830
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)nsv1021334
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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