A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987165



Internal ID12636128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101500374..101834274hg38UCSC Ensembl
Innerchr15:102040577..102374477hg19UCSC Ensembl
Innerchr15:99858100..100192000hg18UCSC Ensembl
Innerchr15:99858100..100192000hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38333901
hg19333901
hg18333901
hg17333901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751544
Supporting Variants
SamplesSPC_100
Known GenesOR4F15, OR4F6, TARSL2, TM2D3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987165
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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