A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509991



Internal ID18808272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121516816..121569846hg38UCSC Ensembl
Innerchr10:123276330..123329360hg19UCSC Ensembl
Innerchr10:123266320..123319350hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3853031
hg1953031
hg1853031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043476
Supporting Variants
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)nssv3509991
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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