A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982718



Internal ID12975444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20217334..20994922hg38UCSC Ensembl
Innerchr15:20422587..21200251hg19UCSC Ensembl
Innerchr15:18682601..19464910hg18UCSC Ensembl
Innerchr15:18682601..19464910hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38777589
hg19777665
hg18782310
hg17782310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751367
Supporting Variants
SamplesBEC_583
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982718
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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