A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066843



Internal ID18809374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78852355..78901892hg38UCSC Ensembl
Innerchr17:76848437..76897974hg19UCSC Ensembl
Innerchr17:74360032..74409569hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3849538
hg1949538
hg1849538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567826
Samples
Known GenesLOC100653515, TIMP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066843
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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