A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983422



Internal ID12976276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108390286..108428802hg38UCSC Ensembl
Innerchr10:110150044..110188560hg19UCSC Ensembl
Innerchr10:110140034..110178550hg18UCSC Ensembl
Innerchr10:110140034..110178550hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3838517
hg1938517
hg1838517
hg1738517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750850
Supporting Variants
SamplesBEC_652
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983422
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