A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508099



Internal ID18459694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97651396..97691104hg38UCSC Ensembl
Innerchr10:99411153..99450861hg19UCSC Ensembl
Innerchr10:99401143..99440851hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3839709
hg1939709
hg1839709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045292
Supporting Variants
Samples
Known GenesAVPI1, PI4K2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508099
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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