A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049497



Internal ID19138716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121526106..121574070hg38UCSC Ensembl
Innerchr10:123285620..123333584hg19UCSC Ensembl
Innerchr10:123275610..123323574hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3847965
hg1947965
hg1847965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv982n100
Supporting Variantsnssv3516028
Samples
Known GenesFGFR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049497
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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