A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065757



Internal ID18808288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81418559..81485298hg38UCSC Ensembl
Innerchr17:79392359..79452324hg19UCSC Ensembl
Innerchr17:77006954..77066919hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3866740
hg1959966
hg1859966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3295n100
Supporting Variantsnssv3567889
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)nsv1065757
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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