A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029373



Internal ID19118592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..375265hg38UCSC Ensembl
Innerchr6:257341..375265hg19UCSC Ensembl
Innerchr6:202341..320265hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38117925
hg19117925
hg18117925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3652412, nssv3652410, nssv3652414, nssv3652411, nssv3652413
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)nsv1029373
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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