A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028592



Internal ID18771123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158281695..158490454hg38UCSC Ensembl
Innerchr6:158702727..158911486hg19UCSC Ensembl
Innerchr6:158622715..158831474hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38208760
hg19208760
hg18208760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749565
Samples
Known GenesTULP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028592
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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