A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981836



Internal ID12974010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93610267..93691367hg38UCSC Ensembl
Innerchr15:94153496..94234596hg19UCSC Ensembl
Innerchr15:91954500..92035600hg18UCSC Ensembl
Innerchr15:91954500..92035600hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3881101
hg1981101
hg1881101
hg1781101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751543
Supporting Variants
SamplesBEC_492
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981836
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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