A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978264



Internal ID12981692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20217334..22270557hg38UCSC Ensembl
Innerchr15:20422587..22558508hg19UCSC Ensembl
Innerchr15:18682601..20059872hg18UCSC Ensembl
Innerchr15:18682601..20059872hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382053224
hg192135922
hg181377272
hg171377272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35107
Supporting Variants
SamplesNA18994
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978264
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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