A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987790



Internal ID12982412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42273163..42349988hg38UCSC Ensembl
Innerchr3:42314655..42391480hg19UCSC Ensembl
Innerchr3:42289659..42366484hg18UCSC Ensembl
Innerchr3:42289659..42366484hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3876826
hg1976826
hg1876826
hg1776826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34472
Supporting Variants
SamplesNA19171
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987790
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