A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985372



Internal ID12983224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19986488..20937641hg38UCSC Ensembl
Innerchr15:20191741..21142970hg19UCSC Ensembl
Innerchr15:18451755..19407629hg18UCSC Ensembl
Innerchr15:18451755..19407629hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38951154
hg19951230
hg18955875
hg17955875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35168
Supporting Variants
SamplesSPC_156
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985372
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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