A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988119



Internal ID12979776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196832482..196917640hg38UCSC Ensembl
Innerchr1:196801612..196886770hg19UCSC Ensembl
Innerchr1:195068235..195153393hg18UCSC Ensembl
Innerchr1:193533269..193618427hg17UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3885159
hg1985159
hg1885159
hg1785159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34776
Supporting Variants
SamplesNA18505
Known GenesCFHR4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988119
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