A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751358



Internal ID12638224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961833..22472558hg38UCSC Ensembl
Innerchr15:20167086..22791936hg19UCSC Ensembl
Innerchr15:18427100..20343300hg18UCSC Ensembl
Innerchr15:18427100..20343300hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382510726
hg192624851
hg181916201
hg171916201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv93e55
Supporting Variantsessv6981740, essv6981741, essv6985662, essv6981742, essv6988445, essv6985663
SamplesBEC_333
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L1, GOLGA6L6, GOLGA8CP, GOLGA8DP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751358
Frequency
Sample Size771
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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