A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984852



Internal ID12983624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35215329..35556000hg38UCSC Ensembl
Innerchr16:34449700..34790371hg19UCSC Ensembl
Innerchr16:34307201..34647872hg18UCSC Ensembl
Innerchr16:34307201..34647872hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38340672
hg19340672
hg18340672
hg17340672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751589
Supporting Variants
SamplesSPC_186
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984852
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