A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985124



Internal ID12636126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101500415..101703151hg38UCSC Ensembl
Innerchr15:102040618..102243354hg19UCSC Ensembl
Innerchr15:99858141..100060877hg18UCSC Ensembl
Innerchr15:99858141..100060877hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38202737
hg19202737
hg18202737
hg17202737
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751544
Supporting Variants
SamplesSPC_100
Known GenesTARSL2, TM2D3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985124
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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