A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024028



Internal ID18766561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5057165..5081756hg38UCSC Ensembl
Innerchr6:5057399..5081990hg19UCSC Ensembl
Innerchr6:5002398..5026989hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3824592
hg1924592
hg1824592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654735
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)nsv1024028
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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