A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066412



Internal ID18808943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68901399..68957926hg38UCSC Ensembl
Innerchr17:66897540..66954067hg19UCSC Ensembl
Innerchr17:64409135..64465662hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3856528
hg1956528
hg1856528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567758
Samples
Known GenesABCA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066412
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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