A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979020



Internal ID12632822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101226272..101432772hg38UCSC Ensembl
Innerchr15:101766477..101972977hg19UCSC Ensembl
Innerchr15:99584000..99790500hg18UCSC Ensembl
Innerchr15:99584000..99790500hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38206501
hg19206501
hg18206501
hg17206501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34275
Supporting Variants
SamplesNA12815
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979020
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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