A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066466



Internal ID18808997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78601694..78666124hg38UCSC Ensembl
Innerchr17:76597776..76662206hg19UCSC Ensembl
Innerchr17:74109371..74173801hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3864431
hg1964431
hg1864431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3285n100
Supporting Variantsnssv3567824
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)nsv1066466
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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