A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058737



Internal ID18801268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81416389..81470706hg38UCSC Ensembl
Innerchr17:79390189..79437732hg19UCSC Ensembl
Innerchr17:77004784..77052327hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3854318
hg1947544
hg1847544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3295n100
Supporting Variantsnssv3567884
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)nsv1058737
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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