A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034080



Internal ID19123302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149135251..149159854hg38UCSC Ensembl
Innerchr6:149456387..149480990hg19UCSC Ensembl
Innerchr6:149498080..149522683hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3824604
hg1924604
hg1824604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654463
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034080
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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