A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988800



Internal ID12630249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6704470..6908200hg38UCSC Ensembl
Innerchr9:6704470..6908200hg19UCSC Ensembl
Innerchr9:6694470..6898200hg18UCSC Ensembl
Innerchr9:6694470..6898200hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38203731
hg19203731
hg18203731
hg17203731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752309
Supporting Variants
SamplesBEC_703
Known GenesKDM4C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988800
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