A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567874



Internal ID18519469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81415451..81457288hg38UCSC Ensembl
Innerchr17:79389251..79424314hg19UCSC Ensembl
Innerchr17:77003846..77038909hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3841838
hg1935064
hg1835064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065921
Supporting Variants
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567874
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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