A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025837



Internal ID18768369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22160366..22227532hg38UCSC Ensembl
Innerchr6:22160595..22227761hg19UCSC Ensembl
Innerchr6:22268574..22335740hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3867167
hg1967167
hg1867167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654824
Samples
Known GenesCASC15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025837
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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