A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561067



Internal ID18859348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34487149..34534367hg38UCSC Ensembl
Innerchr17:32814168..32861386hg19UCSC Ensembl
Innerchr17:29838281..29885499hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3847219
hg1947219
hg1847219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065185
Supporting Variants
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)nssv3561067
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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