A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987333



Internal ID12981497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20908541..20937641hg38UCSC Ensembl
Innerchr15:21113870..21142970hg19UCSC Ensembl
Innerchr15:19378495..19407629hg18UCSC Ensembl
Innerchr15:19378495..19407629hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3829101
hg1929101
hg1829135
hg1729135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751388
Supporting Variants
SamplesNA18971
Known GenesNF1P2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987333
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