A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983781



Internal ID12629240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101300143..101692888hg38UCSC Ensembl
Innerchr10:103059900..103452645hg19UCSC Ensembl
Innerchr10:103049890..103442635hg18UCSC Ensembl
Innerchr10:103049890..103442635hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38392746
hg19392746
hg18392746
hg17392746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750847
Supporting Variants
SamplesBEC_626
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983781
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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