A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv870534



Internal ID16164490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:39709882..39724725hg38UCSC Ensembl
Innerchr17:37866135..37880978hg19UCSC Ensembl
Innerchr17:35119661..35134504hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3814844
hg1914844
hg1814844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574993
Supporting Variants
Samples
Known GenesERBB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv870534
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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