A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983018



Internal ID12627988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6568116..6878215hg38UCSC Ensembl
Innerchr9:6568116..6878215hg19UCSC Ensembl
Innerchr9:6558116..6868215hg18UCSC Ensembl
Innerchr9:6558116..6868215hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38310100
hg19310100
hg18310100
hg17310100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752308
Supporting Variants
SamplesBEC_533
Known GenesGLDC, KDM4C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983018
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