A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987644



Internal ID12983308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65303814..65603718hg38UCSC Ensembl
Innerchr7:64768741..65068631hg19UCSC Ensembl
Innerchr7:64406176..64706066hg18UCSC Ensembl
Innerchr7:64212891..64512781hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38299905
hg19299891
hg18299891
hg17299891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752169
Supporting Variants
SamplesSPC_163
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987644
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