A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567818



Internal ID18866099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77983886..78069603hg38UCSC Ensembl
Innerchr17:75979967..76065684hg19UCSC Ensembl
Innerchr17:73491562..73577279hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3885718
hg1985718
hg1885718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064772
Supporting Variants
Samples
Known GenesTNRC6C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567818
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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