A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984956



Internal ID12983788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20729747..22289825hg38UCSC Ensembl
Innerchr15:20935076..22577776hg19UCSC Ensembl
Innerchr15:19178339..20079140hg18UCSC Ensembl
Innerchr15:19178339..20079140hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381560079
hg191642701
hg18900802
hg17900802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751475
Supporting Variants
SamplesSPC_20
Known GenesCT60, CXADRP2, 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)essv6984956
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer