A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509823



Internal ID18808104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121550511..121566280hg38UCSC Ensembl
Innerchr10:123310025..123325794hg19UCSC Ensembl
Innerchr10:123300015..123315784hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3815770
hg1915770
hg1815770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043313
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)nssv3509823
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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