A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985951



Internal ID12637605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6901229..7103529hg38UCSC Ensembl
Innerchr19:6901240..7103540hg19UCSC Ensembl
Innerchr19:6852240..7054540hg18UCSC Ensembl
Innerchr19:6852240..7054540hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38202301
hg19202301
hg18202301
hg17202301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751808
Supporting Variants
SamplesSPC_87
Known GenesEMR1, EMR4P, FLJ25758, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985951
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