A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029958



Internal ID18772489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22272524..22425932hg38UCSC Ensembl
Innerchr6:22272753..22426161hg19UCSC Ensembl
Innerchr6:22380732..22534140hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38153409
hg19153409
hg18153409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5924n100
Supporting Variantsnssv3654829
Samples
Known GenesPRL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029958
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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