A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981961



Internal ID12974204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65303823..65603737hg38UCSC Ensembl
Innerchr7:64768750..65068650hg19UCSC Ensembl
Innerchr7:64406185..64706085hg18UCSC Ensembl
Innerchr7:64212900..64512800hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38299915
hg19299901
hg18299901
hg17299901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752168
Supporting Variants
SamplesBEC_508
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981961
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