A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017064



Internal ID18759599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38421087..38432979hg38UCSC Ensembl
Innerchr8:38278605..38290497hg19UCSC Ensembl
Innerchr8:38397762..38409654hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3811893
hg1911893
hg1811893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685591
Samples
Known GenesFGFR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017064
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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