A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061314



Internal ID18803845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81415451..81479952hg38UCSC Ensembl
Innerchr17:79389251..79446978hg19UCSC Ensembl
Innerchr17:77003846..77061573hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3864502
hg1957728
hg1857728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3295n100
Supporting Variantsnssv3567882
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)nsv1061314
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer