A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979505



Internal ID12633598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31391871..31506911hg38UCSC Ensembl
Innerchr6:31359648..31474688hg19UCSC Ensembl
Innerchr6:31467627..31582667hg18UCSC Ensembl
Innerchr6:31467627..31582667hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38115041
hg19115041
hg18115041
hg17115041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34684
Supporting Variants
SamplesNA18563
Known GenesHCG26, HCP5, MICA, MICB
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979505
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer