A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017206



Internal ID19106423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..320860hg38UCSC Ensembl
Innerchr6:264744..320860hg19UCSC Ensembl
Innerchr6:209744..265860hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3856117
hg1956117
hg1856117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5885n100
Supporting Variantsnssv3747784
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)nsv1017206
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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